rs373222905
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs373222905(C;T) |
Make rs373222905(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 12 |
Position | 32878332 |
Gene | PKP2 |
is a | snp |
is | mentioned by |
dbSNP | rs373222905 |
dbSNP (classic) | rs373222905 |
ClinGen | rs373222905 |
ebi | rs373222905 |
HLI | rs373222905 |
Exac | rs373222905 |
Gnomad | rs373222905 |
Varsome | rs373222905 |
LitVar | rs373222905 |
Map | rs373222905 |
PheGenI | rs373222905 |
Biobank | rs373222905 |
1000 genomes | rs373222905 |
hgdp | rs373222905 |
ensembl | rs373222905 |
geneview | rs373222905 |
scholar | rs373222905 |
rs373222905 | |
pharmgkb | rs373222905 |
gwascentral | rs373222905 |
openSNP | rs373222905 |
23andMe | rs373222905 |
SNPshot | rs373222905 |
SNPdbe | rs373222905 |
MSV3d | rs373222905 |
GWAS Ctlg | rs373222905 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs373222905(T;T) |
Alt | rs373222905(T;T) |
Reference | Rs373222905(C;C) |
Significance | Pathogenic |
Disease | not specified |
Variation | info |
Gene | PKP2 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000012.11:g.33031266C>T |
CLNSRC | |
CLNACC | RCV000455365.1, |