rs754912778
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs754912778(A;A) |
Make rs754912778(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 12 |
Position | 32869034 |
Gene | PKP2 |
is a | snp |
is | mentioned by |
dbSNP | rs754912778 |
dbSNP (classic) | rs754912778 |
ClinGen | rs754912778 |
ebi | rs754912778 |
HLI | rs754912778 |
Exac | rs754912778 |
Gnomad | rs754912778 |
Varsome | rs754912778 |
LitVar | rs754912778 |
Map | rs754912778 |
PheGenI | rs754912778 |
Biobank | rs754912778 |
1000 genomes | rs754912778 |
hgdp | rs754912778 |
ensembl | rs754912778 |
geneview | rs754912778 |
scholar | rs754912778 |
rs754912778 | |
pharmgkb | rs754912778 |
gwascentral | rs754912778 |
openSNP | rs754912778 |
23andMe | rs754912778 |
SNPshot | rs754912778 |
SNPdbe | rs754912778 |
MSV3d | rs754912778 |
GWAS Ctlg | rs754912778 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs754912778(A;A) |
Alt | rs754912778(A;A) |
Reference | Rs754912778(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | PKP2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000012.11:g.33021968G>A |
CLNSRC | |
CLNACC | RCV000183731.2, |