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rs763818901

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs763818901(A;A)
Make rs763818901(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position179551361
GeneAXDND1, NPHS2
is asnp
is mentioned by
dbSNPrs763818901
dbSNP (old)rs763818901
ClinGenrs763818901
ebirs763818901
HLIrs763818901
Exacrs763818901
Gnomadrs763818901
Varsomers763818901
LitVarrs763818901
Maprs763818901
PheGenIrs763818901
Biobankrs763818901
1000 genomesrs763818901
hgdprs763818901
ensemblrs763818901
gopubmedrs763818901
geneviewrs763818901
scholarrs763818901
googlers763818901
pharmgkbrs763818901
gwascentralrs763818901
openSNPrs763818901
23andMers763818901
23andMe allrs763818901
SNPshotrs763818901
SNPdbers763818901
MSV3drs763818901
GWAS Ctlgrs763818901
Max Magnitude0
ClinVar
Risk rs763818901(A;A)
Alt rs763818901(A;A)
Reference Rs763818901(G;G)
Significance Probable-Pathogenic
Disease Nephrotic syndrome
Variation info
Gene NPHS2 AXDND1
CLNDBN Nephrotic syndrome, idiopathic, steroid-resistant
Reversed 0
HGVS NC_000001.10:g.179520496G>A
CLNSRC
CLNACC RCV000412425.1,