rs41552717
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs41552717(A;A) |
Make rs41552717(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31356845 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs41552717 |
dbSNP (classic) | rs41552717 |
ClinGen | rs41552717 |
ebi | rs41552717 |
HLI | rs41552717 |
Exac | rs41552717 |
Gnomad | rs41552717 |
Varsome | rs41552717 |
LitVar | rs41552717 |
Map | rs41552717 |
PheGenI | rs41552717 |
Biobank | rs41552717 |
1000 genomes | rs41552717 |
hgdp | rs41552717 |
ensembl | rs41552717 |
geneview | rs41552717 |
scholar | rs41552717 |
rs41552717 | |
pharmgkb | rs41552717 |
gwascentral | rs41552717 |
openSNP | rs41552717 |
23andMe | rs41552717 |
SNPshot | rs41552717 |
SNPdbe | rs41552717 |
MSV3d | rs41552717 |
GWAS Ctlg | rs41552717 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs41552717(A;A) rs41552717(G;G) |
Alt | rs41552717(A;A) rs41552717(G;G) |
Reference | Rs41552717(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31324622G>C; NC_000006.11:g.31324622G>T |
CLNSRC | |
CLNACC |