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rs121434390

From SNPedia

Focal segmental glomerulosclerosis 2
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;C) 3.5 Focal segmental glomerulosclerosis 2
(C;C) 0 common in clinvar


Make rs121434390(A;A)
ReferenceGRCh38 38.1/141
Chromosome11
Position101504634
GeneTRPC6
is asnp
is mentioned by
dbSNPrs121434390
ebirs121434390
HLIrs121434390
Exacrs121434390
Varsomers121434390
Maprs121434390
PheGenIrs121434390
hapmaprs121434390
1000 genomesrs121434390
hgdprs121434390
ensemblrs121434390
gopubmedrs121434390
geneviewrs121434390
scholarrs121434390
googlers121434390
pharmgkbrs121434390
gwascentralrs121434390
openSNPrs121434390
23andMers121434390
23andMe allrs121434390
SNP Nexus

SNPshotrs121434390
SNPdbers121434390
MSV3drs121434390
GWAS Ctlgrs121434390
Max Magnitude3.5

Focal segmental glomerulosclerosis

Called i6019082 by 23andMe

OMIM603652
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121434390(A;A)
Alt rs121434390(A;A)
Reference rs121434390(C;C)
Significance Pathogenic
Disease Focal segmental glomerulosclerosis 2
Variation info
Gene TRPC6
CLNDBN Focal segmental glomerulosclerosis 2
Reversed 1
HGVS NC_000011.9:g.101375365G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006526.2,