rs201405287
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs201405287(A;A) |
Make rs201405287(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 12 |
Position | 32822589 |
Gene | PKP2 |
is a | snp |
is | mentioned by |
dbSNP | rs201405287 |
dbSNP (classic) | rs201405287 |
ClinGen | rs201405287 |
ebi | rs201405287 |
HLI | rs201405287 |
Exac | rs201405287 |
Gnomad | rs201405287 |
Varsome | rs201405287 |
LitVar | rs201405287 |
Map | rs201405287 |
PheGenI | rs201405287 |
Biobank | rs201405287 |
1000 genomes | rs201405287 |
hgdp | rs201405287 |
ensembl | rs201405287 |
geneview | rs201405287 |
scholar | rs201405287 |
rs201405287 | |
pharmgkb | rs201405287 |
gwascentral | rs201405287 |
openSNP | rs201405287 |
23andMe | rs201405287 |
SNPshot | rs201405287 |
SNPdbe | rs201405287 |
MSV3d | rs201405287 |
GWAS Ctlg | rs201405287 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs201405287(A;A) |
Alt | rs201405287(A;A) |
Reference | Rs201405287(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | PKP2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000012.11:g.32975523G>A |
CLNSRC | |
CLNACC | RCV000183759.2, |