rs41556617
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs41556617(A;A) |
Make rs41556617(A;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31270009 |
Gene | HLA-C |
is a | snp |
is | mentioned by |
dbSNP | rs41556617 |
dbSNP (classic) | rs41556617 |
ClinGen | rs41556617 |
ebi | rs41556617 |
HLI | rs41556617 |
Exac | rs41556617 |
Gnomad | rs41556617 |
Varsome | rs41556617 |
LitVar | rs41556617 |
Map | rs41556617 |
PheGenI | rs41556617 |
Biobank | rs41556617 |
1000 genomes | rs41556617 |
hgdp | rs41556617 |
ensembl | rs41556617 |
geneview | rs41556617 |
scholar | rs41556617 |
rs41556617 | |
pharmgkb | rs41556617 |
gwascentral | rs41556617 |
openSNP | rs41556617 |
23andMe | rs41556617 |
SNPshot | rs41556617 |
SNPdbe | rs41556617 |
MSV3d | rs41556617 |
GWAS Ctlg | rs41556617 |
GMAF | 0.2429 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs41556617(A;A) |
Alt | rs41556617(A;A) |
Reference | Rs41556617(T;T) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-C |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31237786A>T |
CLNSRC | |
CLNACC |