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rs869312746

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312746(C;T)
Make rs869312746(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position179575750
GeneNPHS2
is asnp
is mentioned by
dbSNPrs869312746
ebirs869312746
HLIrs869312746
Exacrs869312746
Varsomers869312746
Maprs869312746
PheGenIrs869312746
hapmaprs869312746
1000 genomesrs869312746
hgdprs869312746
ensemblrs869312746
gopubmedrs869312746
geneviewrs869312746
scholarrs869312746
googlers869312746
pharmgkbrs869312746
gwascentralrs869312746
openSNPrs869312746
23andMers869312746
23andMe allrs869312746
SNP Nexus

SNPshotrs869312746
SNPdbers869312746
MSV3drs869312746
GWAS Ctlgrs869312746
Max Magnitude0
ClinVar
Risk rs869312746(T;T)
Alt rs869312746(T;T)
Reference rs869312746(C;C)
Significance Pathogenic
Disease Nephrotic syndrome
Variation info
Gene NPHS2
CLNDBN Nephrotic syndrome, idiopathic, steroid-resistant
Reversed 1
HGVS NC_000001.10:g.179544885G>A
CLNSRC
CLNACC RCV000210047.1,