RS10835638 FSHB

Health Risk Chr 11:30230804 snv intron variant

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What This Variant Does

"rs10835638, a SNP located in the (upstream) regulatory region of the follicle stimulating hormone FS...

Associated Conditions

Hypogonadotropic hypogonadism 24 without anosmia

GWAS Studies (2)

Trait	Risk Allele	OR / Beta	P-value	Study
Polycystic ovary syndrome (indeterminate subtype)	T	OR: 1.81	5E-12	PubMed
Follicle stimulating hormone levels in idiopathic male infertility	T	OR: 0.29	6E-7	PubMed

Population Frequencies

1kG AFR

95.3%

1kG ALL

91.6%

1kG AMR

88.3%

1kG EAS

96.8%

1kG EUR

14.3%

1kG SAS

10.3%

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