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

rs1057516880

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057516880(-;TA)
Make rs1057516880(TA;TA)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position179575769
GeneNPHS2
is asnp
is mentioned by
dbSNPrs1057516880
dbSNP (old)rs1057516880
ClinGenrs1057516880
ebirs1057516880
HLIrs1057516880
Exacrs1057516880
Gnomadrs1057516880
Varsomers1057516880
Maprs1057516880
PheGenIrs1057516880
Biobankrs1057516880
1000 genomesrs1057516880
hgdprs1057516880
ensemblrs1057516880
gopubmedrs1057516880
geneviewrs1057516880
scholarrs1057516880
googlers1057516880
pharmgkbrs1057516880
gwascentralrs1057516880
openSNPrs1057516880
23andMers1057516880
23andMe allrs1057516880
SNP Nexus

SNPshotrs1057516880
SNPdbers1057516880
MSV3drs1057516880
GWAS Ctlgrs1057516880
Max Magnitude0
ClinVar
Risk rs1057516880(TA;TA)
Alt rs1057516880(TA;TA)
Reference Rs1057516880(-;-)
Significance Probable-Pathogenic
Disease Nephrotic syndrome
Variation info
Gene NPHS2
CLNDBN Nephrotic syndrome, idiopathic, steroid-resistant
Reversed 1
HGVS NC_000001.10:g.179544904_179544905insTA
CLNSRC
CLNACC RCV000410922.1,