rs41552627
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs41552627(C;T) |
Make rs41552627(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29943203 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs41552627 |
dbSNP (classic) | rs41552627 |
ClinGen | rs41552627 |
ebi | rs41552627 |
HLI | rs41552627 |
Exac | rs41552627 |
Gnomad | rs41552627 |
Varsome | rs41552627 |
LitVar | rs41552627 |
Map | rs41552627 |
PheGenI | rs41552627 |
Biobank | rs41552627 |
1000 genomes | rs41552627 |
hgdp | rs41552627 |
ensembl | rs41552627 |
geneview | rs41552627 |
scholar | rs41552627 |
rs41552627 | |
pharmgkb | rs41552627 |
gwascentral | rs41552627 |
openSNP | rs41552627 |
23andMe | rs41552627 |
SNPshot | rs41552627 |
SNPdbe | rs41552627 |
MSV3d | rs41552627 |
GWAS Ctlg | rs41552627 |
GMAF | 0.06336 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs41552627(T;T) |
Alt | rs41552627(T;T) |
Reference | Rs41552627(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29910980C>T |
CLNSRC | |
CLNACC |