- Chromosome 9

29 variants 3 Drug Response 25 Health Risk 1 Trait

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What This Gene Does
"Variants in the HMG-CoA reductase (HMGCR) gene influence component phenotypes in polycystic ovary syndrome"
Associated Conditions (25)
Levothyroxine response
Statins
attenuated cholesterol lowering by
Chronic obstructive pulmonary disease
Familial prostate cancer
Chronic osteomyelitis
Venous thromboembolism
Radial aplasia-thrombocytopenia syndrome
GPR89B-related condition
Sudden infant death-dysgenesis of the testes syndrome
Choroideremia
Delayed puberty
Intestinal malrotation
Hypogonadotropic hypogonadism 5 with or without anosmia
Autosomal recessive osteopetrosis 7
46
XY sex reversal 1
CHARGE syndrome
Complex cortical dysplasia with other brain malformations 1
XG BLOOD GROUP SYSTEM
+5 more conditions
Key Variants
All Variants (29)
RSID Category Clinical Significance Conditions
RS11185644 Drug Response drug response Levothyroxine response, Levothyroxine response
RS2073547 Drug Response drug response Statins, attenuated cholesterol lowering by, Statins
RS4629571 Drug Response drug response Statins, attenuated cholesterol lowering by, Statins
RS10836312 Health Risk association Chronic obstructive pulmonary disease, Chronic obstructive pulmonary disease
RS188140481 Health Risk association Familial prostate cancer, Familial prostate cancer
RS398652 Health Risk association Chronic osteomyelitis, Chronic osteomyelitis
RS7675998 Health Risk association Chronic osteomyelitis, Chronic osteomyelitis
RS906902 Health Risk association Chronic obstructive pulmonary disease, Chronic obstructive pulmonary disease
RS2853513 Health Risk association not found Venous thromboembolism, Venous thromboembolism
RS61746197 Health Risk Conflicting classifications of pathogenicity Radial aplasia-thrombocytopenia syndrome, GPR89B-related condition, Radial aplasia-thrombocytopenia syndrome
RS2088000353 Health Risk Likely pathogenic Sudden infant death-dysgenesis of the testes syndrome, Sudden infant death-dysgenesis of the testes syndrome, Sudden infant death-dysgenesis of the testes syndrome
RS2147819369 Health Risk Likely pathogenic Choroideremia, Choroideremia
RS727505368 Health Risk Likely pathogenic Delayed puberty, Delayed puberty
RS1567518954 Health Risk Pathogenic Intestinal malrotation, Intestinal malrotation
RS1584891562 Health Risk Pathogenic Hypogonadotropic hypogonadism 5 with or without anosmia, Hypogonadotropic hypogonadism 5 with or without anosmia
RS2144716942 Health Risk Pathogenic Autosomal recessive osteopetrosis 7, Autosomal recessive osteopetrosis 7
RS2521871782 Health Risk Pathogenic 46, XY sex reversal 1, 46
RS2521871783 Health Risk Pathogenic 46, XY sex reversal 1, 46
RS2541435492 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2544633415 Health Risk Pathogenic Complex cortical dysplasia with other brain malformations 1, Complex cortical dysplasia with other brain malformations 1
RS311103 Health Risk Pathogenic XG BLOOD GROUP SYSTEM, Xg(a-) PHENOTYPE, XG BLOOD GROUP SYSTEM
RS483352872 Health Risk Pathogenic Isolated growth hormone deficiency type IB, Isolated growth hormone deficiency type IB
RS527236214 Health Risk Pathogenic
RS6548238 Health Risk risk factor Obesity, Obesity
RS7138803 Health Risk risk factor Obesity, Obesity
RS7711080 Health Risk risk factor Colorectal cancer, Colorectal cancer
RS969095 Health Risk risk factor Colorectal cancer, Colorectal cancer
RS1800955 Health Risk Uncertain risk allele methamphetamine use disorder, methamphetamine use disorder
RS869183622 Trait Affects Venous thromboembolism, Venous thromboembolism
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