ClinVar Miner

List of variants reported as benign for Focal segmental glomerulosclerosis by Illumina Clinical Services Laboratory,Illumina

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ClinVar version:
Total variants: 41
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HGVS dbSNP
NM_004621.6(TRPC6):c.*553T>G rs7931399
NM_004621.6(TRPC6):c.*710_*711insTTTA rs145266305
NM_004621.6(TRPC6):c.-218C>T rs56134796
NM_004621.6(TRPC6):c.-254C>G rs3824934
NM_004621.6(TRPC6):c.-361A>T rs41302375
NM_004621.6(TRPC6):c.1211C>T (p.Ala404Val) rs36111323
NM_004621.6(TRPC6):c.1683T>C (p.Asn561=) rs12366144
NM_004621.6(TRPC6):c.2115C>T (p.Tyr705=) rs61743044
NM_004621.6(TRPC6):c.2529C>T (p.Phe843=) rs72984209
NM_004621.6(TRPC6):c.2712G>A (p.Gln904=) rs12805398
NM_004621.6(TRPC6):c.43C>T (p.Pro15Ser) rs3802829
NM_012120.3(CD2AP):c.*2039T>C rs1043276
NM_012120.3(CD2AP):c.*2228dup rs138722443
NM_012120.3(CD2AP):c.*2339T>C rs2152796
NM_012120.3(CD2AP):c.*2759G>A rs719856
NM_012120.3(CD2AP):c.*367del rs797004904
NM_012120.3(CD2AP):c.*500A>G rs35361796
NM_012120.3(CD2AP):c.*502A>G rs35274349
NM_012120.3(CD2AP):c.-192A>C rs1056434
NM_012120.3(CD2AP):c.-441C>G rs111766401
NM_012120.3(CD2AP):c.-54T>A rs9349406
NM_012120.3(CD2AP):c.1204C>T (p.Leu402=) rs2039503
NM_022489.4(INF2):c.*437G>A rs1128866
NM_022489.4(INF2):c.*536G>T rs1128880
NM_022489.4(INF2):c.-10G>A rs115602636
NM_022489.4(INF2):c.-85G>A rs141884370
NM_022489.4(INF2):c.105C>T (p.Pro35=) rs4983530
NM_022489.4(INF2):c.1227G>T (p.Ser409=) rs3809455
NM_022489.4(INF2):c.2310+8del rs3840006
NM_022489.4(INF2):c.2322C>T (p.Thr774=) rs59751492
NM_022489.4(INF2):c.2571C>T (p.Ser857=) rs62640005
NM_022489.4(INF2):c.2640T>C (p.Asp880=) rs10133301
NM_022489.4(INF2):c.2775+15C>T rs73347508
NM_022489.4(INF2):c.3066T>C (p.Asp1022=) rs4983535
NM_022489.4(INF2):c.3153C>T (p.Asp1051=) rs117457867
NM_022489.4(INF2):c.3207A>C (p.Pro1069=) rs1128840
NM_022489.4(INF2):c.3207A>G (p.Pro1069=) rs1128840
NM_022489.4(INF2):c.3286C>T (p.Pro1096Ser) rs34251364
NM_022489.4(INF2):c.3478G>A (p.Gly1160Ser) rs9672065
NM_022489.4(INF2):c.391+6C>T rs75115369
NM_022489.4(INF2):c.42G>A (p.Leu14=) rs62638758

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