Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057517164

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517164(C;T)
Make rs1057517164(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position179552617
GeneAXDND1, NPHS2
is asnp
is mentioned by
dbSNPrs1057517164
dbSNP (old)rs1057517164
ClinGenrs1057517164
ebirs1057517164
HLIrs1057517164
Exacrs1057517164
Gnomadrs1057517164
Varsomers1057517164
Maprs1057517164
PheGenIrs1057517164
Biobankrs1057517164
1000 genomesrs1057517164
hgdprs1057517164
ensemblrs1057517164
gopubmedrs1057517164
geneviewrs1057517164
scholarrs1057517164
googlers1057517164
pharmgkbrs1057517164
gwascentralrs1057517164
openSNPrs1057517164
23andMers1057517164
23andMe allrs1057517164
SNP Nexus

SNPshotrs1057517164
SNPdbers1057517164
MSV3drs1057517164
GWAS Ctlgrs1057517164
Max Magnitude0
ClinVar
Risk rs1057517164(T;T)
Alt rs1057517164(T;T)
Reference Rs1057517164(C;C)
Significance Probable-Pathogenic
Disease Nephrotic syndrome
Variation info
Gene NPHS2 AXDND1
CLNDBN Nephrotic syndrome, idiopathic, steroid-resistant
Reversed 1
HGVS NC_000001.10:g.179521752G>A
CLNSRC
CLNACC RCV000411647.1,