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rs267606917

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606917(C;C)
Make rs267606917(C;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position35849283
GeneNPHS1
is asnp
is mentioned by
dbSNPrs267606917
ebirs267606917
HLIrs267606917
Exacrs267606917
Varsomers267606917
Maprs267606917
PheGenIrs267606917
hapmaprs267606917
1000 genomesrs267606917
hgdprs267606917
ensemblrs267606917
gopubmedrs267606917
geneviewrs267606917
scholarrs267606917
googlers267606917
pharmgkbrs267606917
gwascentralrs267606917
openSNPrs267606917
23andMers267606917
23andMe allrs267606917
SNP Nexus

SNPshotrs267606917
SNPdbers267606917
MSV3drs267606917
GWAS Ctlgrs267606917
Max Magnitude0
ClinVar
Risk rs267606917(C;C)
Alt rs267606917(C;C)
Reference rs267606917(T;T)
Significance Pathogenic
Disease Finnish congenital nephrotic syndrome
Variation info
Gene NPHS1
CLNDBN Finnish congenital nephrotic syndrome
Reversed 1
HGVS NC_000019.9:g.36340185A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000007277.2,