rs41550613
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs41550613(A;A) |
Make rs41550613(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31271107 |
Gene | HLA-C |
is a | snp |
is | mentioned by |
dbSNP | rs41550613 |
dbSNP (classic) | rs41550613 |
ClinGen | rs41550613 |
ebi | rs41550613 |
HLI | rs41550613 |
Exac | rs41550613 |
Gnomad | rs41550613 |
Varsome | rs41550613 |
LitVar | rs41550613 |
Map | rs41550613 |
PheGenI | rs41550613 |
Biobank | rs41550613 |
1000 genomes | rs41550613 |
hgdp | rs41550613 |
ensembl | rs41550613 |
geneview | rs41550613 |
scholar | rs41550613 |
rs41550613 | |
pharmgkb | rs41550613 |
gwascentral | rs41550613 |
openSNP | rs41550613 |
23andMe | rs41550613 |
SNPshot | rs41550613 |
SNPdbe | rs41550613 |
MSV3d | rs41550613 |
GWAS Ctlg | rs41550613 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs41550613(A;A) |
Alt | rs41550613(A;A) |
Reference | Rs41550613(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-C |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31238884G>T |
CLNSRC | |
CLNACC |