rs41557915
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs41557915(G;T) |
Make rs41557915(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31270119 |
Gene | HLA-C |
is a | snp |
is | mentioned by |
dbSNP | rs41557915 |
dbSNP (classic) | rs41557915 |
ClinGen | rs41557915 |
ebi | rs41557915 |
HLI | rs41557915 |
Exac | rs41557915 |
Gnomad | rs41557915 |
Varsome | rs41557915 |
LitVar | rs41557915 |
Map | rs41557915 |
PheGenI | rs41557915 |
Biobank | rs41557915 |
1000 genomes | rs41557915 |
hgdp | rs41557915 |
ensembl | rs41557915 |
geneview | rs41557915 |
scholar | rs41557915 |
rs41557915 | |
pharmgkb | rs41557915 |
gwascentral | rs41557915 |
openSNP | rs41557915 |
23andMe | rs41557915 |
SNPshot | rs41557915 |
SNPdbe | rs41557915 |
MSV3d | rs41557915 |
GWAS Ctlg | rs41557915 |
GMAF | 0.02571 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs41557915(T;T) |
Alt | rs41557915(T;T) |
Reference | Rs41557915(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-C |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31237896C>A |
CLNSRC | |
CLNACC |