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rs1057516900

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057516900(-;C)
Make rs1057516900(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position179551262
GeneAXDND1, NPHS2
is asnp
is mentioned by
dbSNPrs1057516900
dbSNP (old)rs1057516900
ClinGenrs1057516900
ebirs1057516900
HLIrs1057516900
Exacrs1057516900
Gnomadrs1057516900
Varsomers1057516900
Maprs1057516900
PheGenIrs1057516900
Biobankrs1057516900
1000 genomesrs1057516900
hgdprs1057516900
ensemblrs1057516900
gopubmedrs1057516900
geneviewrs1057516900
scholarrs1057516900
googlers1057516900
pharmgkbrs1057516900
gwascentralrs1057516900
openSNPrs1057516900
23andMers1057516900
23andMe allrs1057516900
SNPshotrs1057516900
SNPdbers1057516900
MSV3drs1057516900
GWAS Ctlgrs1057516900
Max Magnitude0
ClinVar
Risk rs1057516900(C;C)
Alt rs1057516900(C;C)
Reference Rs1057516900(-;-)
Significance Probable-Pathogenic
Disease Nephrotic syndrome
Variation info
Gene NPHS2 AXDND1
CLNDBN Nephrotic syndrome, idiopathic, steroid-resistant
Reversed 1
HGVS NC_000001.10:g.179520398dupG
CLNSRC
CLNACC RCV000411843.1,