rs58606740
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 5 | Polycystic kidney disease, autosomal dominant form (predicted) |
(G;G) | 0 | common in clinvar |
Make rs58606740(A;A) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 4 |
Position | 88038502 |
Gene | PKD2 |
is a | snp |
is | mentioned by |
dbSNP | rs58606740 |
dbSNP (classic) | rs58606740 |
ClinGen | rs58606740 |
ebi | rs58606740 |
HLI | rs58606740 |
Exac | rs58606740 |
Gnomad | rs58606740 |
Varsome | rs58606740 |
LitVar | rs58606740 |
Map | rs58606740 |
PheGenI | rs58606740 |
Biobank | rs58606740 |
1000 genomes | rs58606740 |
hgdp | rs58606740 |
ensembl | rs58606740 |
geneview | rs58606740 |
scholar | rs58606740 |
rs58606740 | |
pharmgkb | rs58606740 |
gwascentral | rs58606740 |
openSNP | rs58606740 |
23andMe | rs58606740 |
SNPshot | rs58606740 |
SNPdbe | rs58606740 |
MSV3d | rs58606740 |
GWAS Ctlg | rs58606740 |
Max Magnitude | 5 |
ClinVar | |
---|---|
Risk | rs58606740(A;A) |
Alt | rs58606740(A;A) |
Reference | Rs58606740(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | PKD2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000004.11:g.88959654G>A |
CLNSRC | |
CLNACC | RCV000379740.1, |