rs41543515
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs41543515(A;A) |
Make rs41543515(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31357145 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs41543515 |
dbSNP (classic) | rs41543515 |
ClinGen | rs41543515 |
ebi | rs41543515 |
HLI | rs41543515 |
Exac | rs41543515 |
Gnomad | rs41543515 |
Varsome | rs41543515 |
LitVar | rs41543515 |
Map | rs41543515 |
PheGenI | rs41543515 |
Biobank | rs41543515 |
1000 genomes | rs41543515 |
hgdp | rs41543515 |
ensembl | rs41543515 |
geneview | rs41543515 |
scholar | rs41543515 |
rs41543515 | |
pharmgkb | rs41543515 |
gwascentral | rs41543515 |
openSNP | rs41543515 |
23andMe | rs41543515 |
SNPshot | rs41543515 |
SNPdbe | rs41543515 |
MSV3d | rs41543515 |
GWAS Ctlg | rs41543515 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs41543515(A;A) |
Alt | rs41543515(A;A) |
Reference | Rs41543515(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31324922G>T |
CLNSRC | |
CLNACC |