rs763818901
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs763818901(A;A) |
Make rs763818901(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 179551361 |
Gene | AXDND1, NPHS2 |
is a | snp |
is | mentioned by |
dbSNP | rs763818901 |
dbSNP (classic) | rs763818901 |
ClinGen | rs763818901 |
ebi | rs763818901 |
HLI | rs763818901 |
Exac | rs763818901 |
Gnomad | rs763818901 |
Varsome | rs763818901 |
LitVar | rs763818901 |
Map | rs763818901 |
PheGenI | rs763818901 |
Biobank | rs763818901 |
1000 genomes | rs763818901 |
hgdp | rs763818901 |
ensembl | rs763818901 |
geneview | rs763818901 |
scholar | rs763818901 |
rs763818901 | |
pharmgkb | rs763818901 |
gwascentral | rs763818901 |
openSNP | rs763818901 |
23andMe | rs763818901 |
SNPshot | rs763818901 |
SNPdbe | rs763818901 |
MSV3d | rs763818901 |
GWAS Ctlg | rs763818901 |
Max Magnitude | 0 |
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, |