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rs74315347

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs74315347(A;A)
Make rs74315347(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position179557227
GeneNPHS2
is asnp
is mentioned by
dbSNPrs74315347
ebirs74315347
HLIrs74315347
Exacrs74315347
Varsomers74315347
Maprs74315347
PheGenIrs74315347
hapmaprs74315347
1000 genomesrs74315347
hgdprs74315347
ensemblrs74315347
gopubmedrs74315347
geneviewrs74315347
scholarrs74315347
googlers74315347
pharmgkbrs74315347
gwascentralrs74315347
openSNPrs74315347
23andMers74315347
23andMe allrs74315347
SNP Nexus

SNPshotrs74315347
SNPdbers74315347
MSV3drs74315347
GWAS Ctlgrs74315347
Max Magnitude0
OMIM604766
Desc
Variant0009
Relatedalso
ClinVar
Risk rs74315347(A;A)
Alt rs74315347(A;A)
Reference rs74315347(G;G)
Significance Other
Disease Nephrotic syndrome
Variation info
Gene NPHS2
CLNDBN Nephrotic syndrome, idiopathic, steroid-resistant
Reversed 1
HGVS NC_000001.10:g.179526362C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005699.4,