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rs1060499703

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499703(A;A)
Make rs1060499703(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position179559762
GeneNPHS2
is asnp
is mentioned by
dbSNPrs1060499703
dbSNP (old)rs1060499703
ClinGenrs1060499703
ebirs1060499703
HLIrs1060499703
Exacrs1060499703
Gnomadrs1060499703
Varsomers1060499703
LitVarrs1060499703
Maprs1060499703
PheGenIrs1060499703
Biobankrs1060499703
1000 genomesrs1060499703
hgdprs1060499703
ensemblrs1060499703
gopubmedrs1060499703
geneviewrs1060499703
scholarrs1060499703
googlers1060499703
pharmgkbrs1060499703
gwascentralrs1060499703
openSNPrs1060499703
23andMers1060499703
23andMe allrs1060499703
SNPshotrs1060499703
SNPdbers1060499703
MSV3drs1060499703
GWAS Ctlgrs1060499703
Max Magnitude0
ClinVar
Risk rs1060499703(A;A)
Alt rs1060499703(A;A)
Reference Rs1060499703(G;G)
Significance Pathogenic
Disease Nephrotic syndrome
Variation info
Gene NPHS2
CLNDBN Nephrotic syndrome, idiopathic, steroid-resistant
Reversed 1
HGVS NC_000001.10:g.179528897C>T
CLNSRC
CLNACC RCV000449520.1,