rs41540512
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs41540512(C;G) |
Make rs41540512(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31269997 |
Gene | HLA-C |
is a | snp |
is | mentioned by |
dbSNP | rs41540512 |
dbSNP (classic) | rs41540512 |
ClinGen | rs41540512 |
ebi | rs41540512 |
HLI | rs41540512 |
Exac | rs41540512 |
Gnomad | rs41540512 |
Varsome | rs41540512 |
LitVar | rs41540512 |
Map | rs41540512 |
PheGenI | rs41540512 |
Biobank | rs41540512 |
1000 genomes | rs41540512 |
hgdp | rs41540512 |
ensembl | rs41540512 |
geneview | rs41540512 |
scholar | rs41540512 |
rs41540512 | |
pharmgkb | rs41540512 |
gwascentral | rs41540512 |
openSNP | rs41540512 |
23andMe | rs41540512 |
SNPshot | rs41540512 |
SNPdbe | rs41540512 |
MSV3d | rs41540512 |
GWAS Ctlg | rs41540512 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs41540512(G;G) |
Alt | rs41540512(G;G) |
Reference | Rs41540512(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-C |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31237774G>C |
CLNSRC | |
CLNACC |