SNP Directory

450,817 genetic variants in our database.

All (450,817) Health Risk (400,964) Other (47,777) Drug Response (1,898) Trait (128) Protective (50)
RSID Gene Category Clinical Significance Conditions
RS730880942 MYL2 Health Risk Conflicting classifications of pathogenicity Hypertrophic cardiomyopathy 10, Cardiomyopathy
RS730880944 MYL2 Health Risk Conflicting classifications of pathogenicity Hypertrophic cardiomyopathy, Hypertrophic cardiomyopathy 10
RS730880946 MYL2 Health Risk Conflicting classifications of pathogenicity Hypertrophic cardiomyopathy 10, Cardiovascular phenotype
RS730880948 MYL2 Health Risk Conflicting classifications of pathogenicity Hypertrophic cardiomyopathy 10, Cardiovascular phenotype
RS730880952 MYL2 Health Risk Likely pathogenic —
RS730880956 MYL3 Health Risk Conflicting classifications of pathogenicity Hypertrophic cardiomyopathy 8, Cardiomyopathy
RS730880960 MYL3 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Cardiovascular phenotype
RS730880962 MYL3 Health Risk Conflicting classifications of pathogenicity Hypertrophic cardiomyopathy, Hypertrophic cardiomyopathy
RS730880963 NPC1 Health Risk Pathogenic/Likely pathogenic Niemann-Pick disease, type C1
RS730880965 NRAS Health Risk Conflicting classifications of pathogenicity Noonan syndrome 6, Cardiovascular phenotype
RS730880967 NRAS Health Risk Pathogenic RASopathy, RASopathy
RS730880971 PRKAG2 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Lethal congenital glycogen storage disease of heart
RS730880972 PRKAG2 Health Risk Conflicting classifications of pathogenicity Lethal congenital glycogen storage disease of heart, Cardiovascular phenotype
RS730880975 PRKAG2 Health Risk Conflicting classifications of pathogenicity Wolff-Parkinson-White pattern, Cardiomyopathy
RS730880978 PRKAG2 Health Risk Conflicting classifications of pathogenicity Lethal congenital glycogen storage disease of heart, Cardiomyopathy
RS730880987 PRKAG2 Health Risk Conflicting classifications of pathogenicity Lethal congenital glycogen storage disease of heart, Cardiomyopathy
RS730880989 PRKAG2 Health Risk Conflicting classifications of pathogenicity Lethal congenital glycogen storage disease of heart, Cardiomyopathy
RS730880998 RAF1 Health Risk Conflicting classifications of pathogenicity —
RS730881000 RAF1 Health Risk Conflicting classifications of pathogenicity RASopathy, Cardiovascular phenotype
RS730881002 RAF1 Health Risk Pathogenic/Likely pathogenic Noonan syndrome and Noonan-related syndrome, RASopathy
RS730881003 RAF1 Health Risk Pathogenic/Likely pathogenic Noonan syndrome, RASopathy
RS730881006 RAF1 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, RASopathy
RS730881007 RAF1 Health Risk Conflicting classifications of pathogenicity RASopathy, Cardiovascular phenotype
RS730881009 RAF1 Health Risk Likely pathogenic —
RS730881010 RAF1 Health Risk Likely pathogenic RASopathy, RASopathy
RS730881012 RIT1 Health Risk Conflicting classifications of pathogenicity Noonan syndrome 8, Noonan syndrome 8
RS730881014 RIT1 Health Risk Pathogenic Noonan syndrome 8, Noonan syndrome
RS730881017 SHOC2 Health Risk Conflicting classifications of pathogenicity RASopathy, Cardiovascular phenotype
RS730881019 SHOC2 Health Risk Conflicting classifications of pathogenicity RASopathy, Noonan syndrome-like disorder with loose anagen hair 1
RS730881020 SHOC2 Health Risk Pathogenic Noonan syndrome-like disorder with loose anagen hair 1, RASopathy
RS730881024 SOS1 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Cardiovascular phenotype
RS730881026 SOS1 Health Risk Conflicting classifications of pathogenicity RASopathy, Noonan syndrome and Noonan-related syndrome
RS730881031 SOS1 Health Risk Conflicting classifications of pathogenicity RASopathy, Cardiovascular phenotype
RS730881032 SOS1 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, RASopathy
RS730881034 SOS1 Health Risk Conflicting classifications of pathogenicity RASopathy, Fibromatosis
RS730881035 SOS1 Health Risk Conflicting classifications of pathogenicity RASopathy, Noonan syndrome 4
RS730881036 SOS1 Health Risk Conflicting classifications of pathogenicity Noonan syndrome 4, Fibromatosis
RS730881038 SOS1 Health Risk Conflicting classifications of pathogenicity RASopathy, Fibromatosis
RS730881041 SOS1 Health Risk Likely pathogenic —
RS730881042 SOS1 Health Risk Conflicting classifications of pathogenicity RASopathy, Noonan syndrome 4
RS730881044 SOS1 Health Risk Pathogenic/Likely pathogenic Noonan syndrome 4, Fibromatosis
RS730881045 SOS1 Health Risk Pathogenic/Likely pathogenic Noonan syndrome, RASopathy
RS730881046 SOS1 Health Risk Conflicting classifications of pathogenicity RASopathy, Cardiovascular phenotype
RS730881048 SOS1 Health Risk Pathogenic RASopathy, RASopathy
RS730881051 SOS1 Health Risk Conflicting classifications of pathogenicity RASopathy, Cardiovascular phenotype
RS730881053 SOS1 Health Risk Conflicting classifications of pathogenicity RASopathy, Fibromatosis
RS730881054 SOS1 Health Risk Pathogenic/Likely pathogenic RASopathy, Noonan syndrome
RS730881058 TNNC1 Health Risk Conflicting classifications of pathogenicity Hypertrophic cardiomyopathy 13, Dilated cardiomyopathy 1Z
RS730881059 TNNC1 Health Risk Likely pathogenic —
RS730881061 TNNC1 Health Risk Conflicting classifications of pathogenicity Dilated cardiomyopathy 1Z, Hypertrophic cardiomyopathy 13
RS730881063 TNNC1 Health Risk Likely pathogenic —
RS730881065 TNNC1 Health Risk Conflicting classifications of pathogenicity Hypertrophic cardiomyopathy 13, Dilated cardiomyopathy 1Z
RS730881066 TNNI3 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Hypertrophic cardiomyopathy
RS730881068 TNNI3 Health Risk Conflicting classifications of pathogenicity Hypertrophic cardiomyopathy, Cardiomyopathy
RS730881069 TNNI3 Health Risk Conflicting classifications of pathogenicity Hypertrophic cardiomyopathy, Cardiomyopathy
RS730881070 TNNI3 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Hypertrophic cardiomyopathy
RS730881071 TNNI3 Health Risk Conflicting classifications of pathogenicity Hypertrophic cardiomyopathy, Cardiomyopathy
RS730881075 TNNI3 Health Risk Likely pathogenic —
RS730881076 TNNI3 Health Risk Likely pathogenic —
RS730881077 TNNI3 Health Risk Pathogenic —
RS730881078 TNNI3 Health Risk Pathogenic TNNI3-related disorder, TNNI3-related disorder
RS730881079 TNNI3 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Hypertrophic cardiomyopathy
RS730881081 TNNI3 Health Risk Conflicting classifications of pathogenicity Hypertrophic cardiomyopathy, Hypertrophic cardiomyopathy
RS730881082 TNNI3 Health Risk Pathogenic —
RS730881083 TNNI3 Health Risk Conflicting classifications of pathogenicity Hypertrophic cardiomyopathy, Cardiovascular phenotype
RS730881085 TNNI3 Health Risk Conflicting classifications of pathogenicity Hypertrophic cardiomyopathy, Cardiovascular phenotype
RS730881086 TNNI3 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Hypertrophic cardiomyopathy
RS730881087 TNNI3 Health Risk Conflicting classifications of pathogenicity Hypertrophic cardiomyopathy 7, Dilated cardiomyopathy 1FF
RS730881090 TNNI3 Health Risk Likely pathogenic —
RS730881091 TNNI3 Health Risk Pathogenic/Likely pathogenic Hypertrophic cardiomyopathy 7, Hypertrophic cardiomyopathy
RS730881092 TNNT2 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Hypertrophic cardiomyopathy 2
RS730881093 TNNT2 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Dilated cardiomyopathy 1D
RS730881096 TNNT2 Health Risk Conflicting classifications of pathogenicity Dilated cardiomyopathy 1D, Cardiomyopathy
RS730881097 TNNT2 Health Risk Conflicting classifications of pathogenicity Primary dilated cardiomyopathy, Dilated cardiomyopathy 1D
RS730881098 TNNT2 Health Risk Pathogenic Hypertrophic cardiomyopathy 2, Dilated cardiomyopathy 1D
RS730881101 TNNT2 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Hypertrophic cardiomyopathy 2
RS730881103 TNNT2 Health Risk Conflicting classifications of pathogenicity Dilated cardiomyopathy 1D, Cardiomyopathy
RS730881104 TNNT2 Health Risk Likely pathogenic —
RS730881106 TNNT2 Health Risk Conflicting classifications of pathogenicity Dilated cardiomyopathy 1D, Cardiomyopathy
RS730881115 TNNT2 Health Risk Conflicting classifications of pathogenicity Dilated cardiomyopathy 1D, Cardiovascular phenotype
RS730881116 TNNT2 Health Risk Pathogenic/Likely pathogenic Cardiovascular phenotype, Hypertrophic cardiomyopathy
RS730881119 TNNT2 Health Risk Pathogenic Cardiomyopathy, Cardiomyopathy
RS730881120 TNNT2 Health Risk Conflicting classifications of pathogenicity Hypertrophic cardiomyopathy 2, Dilated cardiomyopathy 1D
RS730881121 TNNT2 Health Risk Pathogenic —
RS730881122 TNNT2 Health Risk Conflicting classifications of pathogenicity Hypertrophic cardiomyopathy, Dilated cardiomyopathy 1D
RS730881124 TNNT2 Health Risk Conflicting classifications of pathogenicity Dilated cardiomyopathy 1D, Cardiomyopathy
RS730881128 TPM1 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Cardiomyopathy
RS730881131 TPM1 Health Risk Pathogenic/Likely pathogenic Hypertrophic cardiomyopathy, Hypertrophic cardiomyopathy 3
RS730881132 TPM1 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Cardiomyopathy
RS730881134 TPM1 Health Risk Conflicting classifications of pathogenicity Hypertrophic cardiomyopathy, Hypertrophic cardiomyopathy
RS730881136 TPM1 Health Risk Conflicting classifications of pathogenicity Hypertrophic cardiomyopathy, Hypertrophic cardiomyopathy
RS730881140 TPM1 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Hypertrophic cardiomyopathy
RS730881141 TPM1 Health Risk Conflicting classifications of pathogenicity Hypertrophic cardiomyopathy, Cardiovascular phenotype
RS730881151 TPM1 Health Risk Conflicting classifications of pathogenicity Hypertrophic cardiomyopathy 3, Cardiovascular phenotype
RS730881157 TPM1 Health Risk Pathogenic —
RS730881159 TPM1 Health Risk Conflicting classifications of pathogenicity Hypertrophic cardiomyopathy, Hypertrophic cardiomyopathy
RS730881160 TPM1 Health Risk Conflicting classifications of pathogenicity Hypertrophic cardiomyopathy, Hypertrophic cardiomyopathy
RS730881162 TTR Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Hyperthyroxinemia
RS730881163 TTR Health Risk Pathogenic/Likely pathogenic Amyloidosis, hereditary systemic 1
RS730881164 TTR Health Risk Conflicting classifications of pathogenicity Amyloidosis, hereditary systemic 1
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