rs41546813
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs41546813(A;A) |
Make rs41546813(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31271586 |
Gene | HLA-C |
is a | snp |
is | mentioned by |
dbSNP | rs41546813 |
dbSNP (classic) | rs41546813 |
ClinGen | rs41546813 |
ebi | rs41546813 |
HLI | rs41546813 |
Exac | rs41546813 |
Gnomad | rs41546813 |
Varsome | rs41546813 |
LitVar | rs41546813 |
Map | rs41546813 |
PheGenI | rs41546813 |
Biobank | rs41546813 |
1000 genomes | rs41546813 |
hgdp | rs41546813 |
ensembl | rs41546813 |
geneview | rs41546813 |
scholar | rs41546813 |
rs41546813 | |
pharmgkb | rs41546813 |
gwascentral | rs41546813 |
openSNP | rs41546813 |
23andMe | rs41546813 |
SNPshot | rs41546813 |
SNPdbe | rs41546813 |
MSV3d | rs41546813 |
GWAS Ctlg | rs41546813 |
GMAF | 0.0225 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs41546813(A;A) |
Alt | rs41546813(A;A) |
Reference | Rs41546813(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-C |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31239363C>T |
CLNSRC | |
CLNACC |