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rs1057516395

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057516395(-;-)
Make rs1057516395(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position179564699
GeneNPHS2
is asnp
is mentioned by
dbSNPrs1057516395
dbSNP (old)rs1057516395
ClinGenrs1057516395
ebirs1057516395
HLIrs1057516395
Exacrs1057516395
Gnomadrs1057516395
Varsomers1057516395
Maprs1057516395
PheGenIrs1057516395
Biobankrs1057516395
1000 genomesrs1057516395
hgdprs1057516395
ensemblrs1057516395
gopubmedrs1057516395
geneviewrs1057516395
scholarrs1057516395
googlers1057516395
pharmgkbrs1057516395
gwascentralrs1057516395
openSNPrs1057516395
23andMers1057516395
23andMe allrs1057516395
SNP Nexus

SNPshotrs1057516395
SNPdbers1057516395
MSV3drs1057516395
GWAS Ctlgrs1057516395
Max Magnitude0
ClinVar
Risk rs1057516395(-;-)
Alt rs1057516395(-;-)
Reference Rs1057516395(C;C)
Significance Probable-Pathogenic
Disease Nephrotic syndrome
Variation info
Gene NPHS2
CLNDBN Nephrotic syndrome, idiopathic, steroid-resistant
Reversed 1
HGVS NC_000001.10:g.179533834delG
CLNSRC
CLNACC RCV000412170.1,