rs201494226
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs201494226(A;A) |
Make rs201494226(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 167518400 |
Gene | CD247 |
is a | snp |
is | mentioned by |
dbSNP | rs201494226 |
dbSNP (classic) | rs201494226 |
ClinGen | rs201494226 |
ebi | rs201494226 |
HLI | rs201494226 |
Exac | rs201494226 |
Gnomad | rs201494226 |
Varsome | rs201494226 |
LitVar | rs201494226 |
Map | rs201494226 |
PheGenI | rs201494226 |
Biobank | rs201494226 |
1000 genomes | rs201494226 |
hgdp | rs201494226 |
ensembl | rs201494226 |
geneview | rs201494226 |
scholar | rs201494226 |
rs201494226 | |
pharmgkb | rs201494226 |
gwascentral | rs201494226 |
openSNP | rs201494226 |
23andMe | rs201494226 |
SNPshot | rs201494226 |
SNPdbe | rs201494226 |
MSV3d | rs201494226 |
GWAS Ctlg | rs201494226 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs201494226(A;A) |
Alt | rs201494226(A;A) |
Reference | Rs201494226(G;G) |
Significance | Probable-Pathogenic |
Disease | not specified |
Variation | info |
Gene | CD247 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000001.10:g.167487637G>A |
CLNSRC | |
CLNACC | RCV000171161.2, |