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rs74315342

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs74315342(A;A)
Make rs74315342(A;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position179561327
GeneNPHS2
is asnp
is mentioned by
dbSNPrs74315342
ebirs74315342
HLIrs74315342
Exacrs74315342
Varsomers74315342
Maprs74315342
PheGenIrs74315342
hapmaprs74315342
1000 genomesrs74315342
hgdprs74315342
ensemblrs74315342
gopubmedrs74315342
geneviewrs74315342
scholarrs74315342
googlers74315342
pharmgkbrs74315342
gwascentralrs74315342
openSNPrs74315342
23andMers74315342
23andMe allrs74315342
SNP Nexus

SNPshotrs74315342
SNPdbers74315342
MSV3drs74315342
GWAS Ctlgrs74315342
Max Magnitude0
OMIM604766
Desc
Variant0001
Relatedalso
ClinVar
Risk rs74315342(A;A)
Alt rs74315342(A;A)
Reference rs74315342(G;G)
Significance Pathogenic
Disease Nephrotic syndrome
Variation info
Gene NPHS2
CLNDBN Nephrotic syndrome, idiopathic, steroid-resistant
Reversed 1
HGVS NC_000001.10:g.179530462C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005691.2,