rs41540614
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs41540614(C;G) |
Make rs41540614(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29943088 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs41540614 |
dbSNP (classic) | rs41540614 |
ClinGen | rs41540614 |
ebi | rs41540614 |
HLI | rs41540614 |
Exac | rs41540614 |
Gnomad | rs41540614 |
Varsome | rs41540614 |
LitVar | rs41540614 |
Map | rs41540614 |
PheGenI | rs41540614 |
Biobank | rs41540614 |
1000 genomes | rs41540614 |
hgdp | rs41540614 |
ensembl | rs41540614 |
geneview | rs41540614 |
scholar | rs41540614 |
rs41540614 | |
pharmgkb | rs41540614 |
gwascentral | rs41540614 |
openSNP | rs41540614 |
23andMe | rs41540614 |
SNPshot | rs41540614 |
SNPdbe | rs41540614 |
MSV3d | rs41540614 |
GWAS Ctlg | rs41540614 |
GMAF | 0.08861 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs41540614(G;G) |
Alt | rs41540614(G;G) |
Reference | Rs41540614(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29910865C>G |
CLNSRC | |
CLNACC |