RS138908576 ADGRV1

Health Risk Chr 5:90774248 snv missense variant
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Associated Conditions
Febrile seizures
familial
4
Usher syndrome type 2C
Usher syndrome type 2
ADGRV1-related disorder
Inborn genetic diseases
Febrile seizures
familial
4
Usher syndrome type 2C
Usher syndrome type 2
ADGRV1-related disorder
Inborn genetic diseases
Population Frequencies
gnomAD ALL
0%
1kG AFR
100%
1kG ALL
100%
1kG AMR
100%
1kG EAS
99.9%
1kG EUR
100%
1kG SAS
100%
Other Variants in ADGRV1
rs121909761 rs121909762 rs796051863 rs796051864 rs796051865 rs121909763 rs796051866 rs796051867 rs1554135663 rs397517418
Ask Dr. Hemsworth about this variant