ClinVar Miner

List of variants in gene TRPC6 reported as likely benign for focal segmental glomerulosclerosis 2

Included ClinVar conditions (1):
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Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_004621.6(TRPC6):c.2088C>T (p.Asn696=) rs61739601 0.00743
NM_004621.6(TRPC6):c.1818T>C (p.Ser606=) rs139187399 0.00222
NM_004621.6(TRPC6):c.948T>C (p.Asn316=) rs139477687 0.00035
NM_004621.6(TRPC6):c.253_264dup (p.Ala85_Phe88dup) rs778276152 0.00029
NM_004621.6(TRPC6):c.888G>A (p.Thr296=) rs144891994 0.00029
NM_004621.6(TRPC6):c.374A>G (p.Asn125Ser) rs146776939 0.00022
NM_004621.6(TRPC6):c.996C>T (p.Leu332=) rs200144852 0.00021
NM_004621.6(TRPC6):c.336A>C (p.Pro112=) rs201818043 0.00010
NM_004621.6(TRPC6):c.667A>G (p.Ile223Val) rs150033580 0.00010
NM_004621.6(TRPC6):c.1899C>T (p.Asp633=) rs187196477 0.00007
NM_004621.6(TRPC6):c.1094G>A (p.Arg365His) rs755825482 0.00005
NM_004621.6(TRPC6):c.213T>A (p.Val71=) rs138123801 0.00004
NM_004621.6(TRPC6):c.1294-4G>A rs190191809 0.00003
NM_004621.6(TRPC6):c.2409+19T>G rs147856182 0.00003
NM_004621.6(TRPC6):c.2488G>A (p.Gly830Arg) rs199810047 0.00003
NM_004621.6(TRPC6):c.*3C>T rs199566055 0.00001
NM_004621.6(TRPC6):c.1212G>A (p.Ala404=) rs144085223
NM_004621.6(TRPC6):c.2142G>A (p.Thr714=) rs145077205
NM_004621.6(TRPC6):c.273C>T (p.Arg91=) rs140496742
NM_004621.6(TRPC6):c.905A>G (p.Asn302Ser)

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