RS117273916 TRPC6

Health Risk Chr 11:101504796 snv missense variant

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Associated Conditions

Focal segmental glomerulosclerosis 2

Inborn genetic diseases

Focal segmental glomerulosclerosis 2

Inborn genetic diseases

Population Frequencies

gnomAD ALL

99.9%

1kG AFR

0.1%

1kG ALL

99.9%

1kG AMR

100%

1kG EAS

99.9%

1kG EUR

99.8%

1kG SAS

100%

Other Variants in TRPC6