rs145877597
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 5 | Polycystic kidney disease, autosomal dominant form (predicted) |
(G;G) | 0 | common/normal |
Make rs145877597(A;A) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 4 |
Position | 88038372 |
Gene | PKD2 |
is a | snp |
is | mentioned by |
dbSNP | rs145877597 |
dbSNP (classic) | rs145877597 |
ClinGen | rs145877597 |
ebi | rs145877597 |
HLI | rs145877597 |
Exac | rs145877597 |
Gnomad | rs145877597 |
Varsome | rs145877597 |
LitVar | rs145877597 |
Map | rs145877597 |
PheGenI | rs145877597 |
Biobank | rs145877597 |
1000 genomes | rs145877597 |
hgdp | rs145877597 |
ensembl | rs145877597 |
geneview | rs145877597 |
scholar | rs145877597 |
rs145877597 | |
pharmgkb | rs145877597 |
gwascentral | rs145877597 |
openSNP | rs145877597 |
23andMe | rs145877597 |
SNPshot | rs145877597 |
SNPdbe | rs145877597 |
MSV3d | rs145877597 |
GWAS Ctlg | rs145877597 |
Max Magnitude | 5 |
Listed as highly likely to be pathogenic in the Autosomal Polycystic Kidney Disease database.
23andMe name: i5047404