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rs869025495

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025495(C;T)
Make rs869025495(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position179564715
GeneNPHS2
is asnp
is mentioned by
dbSNPrs869025495
ebirs869025495
HLIrs869025495
Exacrs869025495
Varsomers869025495
Maprs869025495
PheGenIrs869025495
hapmaprs869025495
1000 genomesrs869025495
hgdprs869025495
ensemblrs869025495
gopubmedrs869025495
geneviewrs869025495
scholarrs869025495
googlers869025495
pharmgkbrs869025495
gwascentralrs869025495
openSNPrs869025495
23andMers869025495
23andMe allrs869025495
SNP Nexus

SNPshotrs869025495
SNPdbers869025495
MSV3drs869025495
GWAS Ctlgrs869025495
Max Magnitude0
ClinVar
Risk rs869025495(T;T)
Alt rs869025495(T;T)
Reference rs869025495(C;C)
Significance Pathogenic
Disease Proteinuria
Variation info
Gene NPHS2
CLNDBN Proteinuria
Reversed 1
HGVS NC_000001.10:g.179533850G>A
CLNSRC
CLNACC RCV000208227.1,