RS138886378 TRPM1

Health Risk Chr 15:31067144 snv missense variant

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Associated Conditions

Congenital stationary night blindness 1C

Retinitis pigmentosa

TRPM1-related disorder

Congenital stationary night blindness 1C

Retinitis pigmentosa

TRPM1-related disorder

Population Frequencies

gnomAD ALL

99.6%

1kG AFR

100%

1kG ALL

0.1%

1kG AMR

0.3%

1kG EAS

100%

1kG EUR

99.7%

1kG SAS

100%

Other Variants in TRPM1