rs794729106
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs794729106(C;C) |
Make rs794729106(C;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 12 |
Position | 32850766 |
Gene | PKP2 |
is a | snp |
is | mentioned by |
dbSNP | rs794729106 |
dbSNP (classic) | rs794729106 |
ClinGen | rs794729106 |
ebi | rs794729106 |
HLI | rs794729106 |
Exac | rs794729106 |
Gnomad | rs794729106 |
Varsome | rs794729106 |
LitVar | rs794729106 |
Map | rs794729106 |
PheGenI | rs794729106 |
Biobank | rs794729106 |
1000 genomes | rs794729106 |
hgdp | rs794729106 |
ensembl | rs794729106 |
geneview | rs794729106 |
scholar | rs794729106 |
rs794729106 | |
pharmgkb | rs794729106 |
gwascentral | rs794729106 |
openSNP | rs794729106 |
23andMe | rs794729106 |
SNPshot | rs794729106 |
SNPdbe | rs794729106 |
MSV3d | rs794729106 |
GWAS Ctlg | rs794729106 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs794729106(C;C) |
Alt | rs794729106(C;C) |
Reference | Rs794729106(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | PKP2 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000012.11:g.33003700C>G |
CLNSRC | |
CLNACC | RCV000183742.1, |