rs794729116
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs794729116(A;A) |
Make rs794729116(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 12 |
Position | 32802402 |
Gene | PKP2 |
is a | snp |
is | mentioned by |
dbSNP | rs794729116 |
dbSNP (classic) | rs794729116 |
ClinGen | rs794729116 |
ebi | rs794729116 |
HLI | rs794729116 |
Exac | rs794729116 |
Gnomad | rs794729116 |
Varsome | rs794729116 |
LitVar | rs794729116 |
Map | rs794729116 |
PheGenI | rs794729116 |
Biobank | rs794729116 |
1000 genomes | rs794729116 |
hgdp | rs794729116 |
ensembl | rs794729116 |
geneview | rs794729116 |
scholar | rs794729116 |
rs794729116 | |
pharmgkb | rs794729116 |
gwascentral | rs794729116 |
openSNP | rs794729116 |
23andMe | rs794729116 |
SNPshot | rs794729116 |
SNPdbe | rs794729116 |
MSV3d | rs794729116 |
GWAS Ctlg | rs794729116 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs794729116(A;A) rs794729116(T;T) |
Alt | rs794729116(A;A) rs794729116(T;T) |
Reference | Rs794729116(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | PKP2 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000012.11:g.32955336C>T |
CLNSRC | |
CLNACC | RCV000183774.2, |