rs794729128
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
(I;I) | 0 | common genotype |
Make rs794729128(-;-) |
Make rs794729128(-;A) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 12 |
Position | 32824052 |
Gene | PKP2 |
is a | snp |
is | mentioned by |
dbSNP | rs794729128 |
dbSNP (classic) | rs794729128 |
ClinGen | rs794729128 |
ebi | rs794729128 |
HLI | rs794729128 |
Exac | rs794729128 |
Gnomad | rs794729128 |
Varsome | rs794729128 |
LitVar | rs794729128 |
Map | rs794729128 |
PheGenI | rs794729128 |
Biobank | rs794729128 |
1000 genomes | rs794729128 |
hgdp | rs794729128 |
ensembl | rs794729128 |
geneview | rs794729128 |
scholar | rs794729128 |
rs794729128 | |
pharmgkb | rs794729128 |
gwascentral | rs794729128 |
openSNP | rs794729128 |
23andMe | rs794729128 |
SNPshot | rs794729128 |
SNPdbe | rs794729128 |
MSV3d | rs794729128 |
GWAS Ctlg | rs794729128 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs794729128(-;-) |
Alt | rs794729128(-;-) |
Reference | Rs794729128(A;A) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | PKP2 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000012.11:g.32976986delT |
CLNSRC | |
CLNACC | RCV000183793.1, |