RS137871935 SEMA3A

Health Risk Chr 7:84001956 snv missense variant

Upload your DNA to see your genotype for this variant.

Associated Conditions

SEMA3A-related disorder

Hypogonadotropic hypogonadism 16 with or without anosmia

Male infertility with azoospermia or oligozoospermia due to single gene mutation

SEMA3A-related disorder

Hypogonadotropic hypogonadism 16 with or without anosmia

Male infertility with azoospermia or oligozoospermia due to single gene mutation

Population Frequencies

gnomAD ALL

100%

1kG AFR

100%

1kG ALL

100%

1kG AMR

100%

1kG EAS

100%

1kG EUR

0.2%

1kG SAS

100%

Other Variants in SEMA3A