rs41554614
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs41554614(C;T) |
Make rs41554614(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29942730 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs41554614 |
dbSNP (classic) | rs41554614 |
ClinGen | rs41554614 |
ebi | rs41554614 |
HLI | rs41554614 |
Exac | rs41554614 |
Gnomad | rs41554614 |
Varsome | rs41554614 |
LitVar | rs41554614 |
Map | rs41554614 |
PheGenI | rs41554614 |
Biobank | rs41554614 |
1000 genomes | rs41554614 |
hgdp | rs41554614 |
ensembl | rs41554614 |
geneview | rs41554614 |
scholar | rs41554614 |
rs41554614 | |
pharmgkb | rs41554614 |
gwascentral | rs41554614 |
openSNP | rs41554614 |
23andMe | rs41554614 |
SNPshot | rs41554614 |
SNPdbe | rs41554614 |
MSV3d | rs41554614 |
GWAS Ctlg | rs41554614 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs41554614(T;T) |
Alt | rs41554614(T;T) |
Reference | Rs41554614(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29910507C>T |
CLNSRC | |
CLNACC |