rs1136659
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs1136659(A;A) |
Make rs1136659(A;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 29942780 |
Gene | HLA-A |
is a | snp |
is | mentioned by |
dbSNP | rs1136659 |
dbSNP (classic) | rs1136659 |
ClinGen | rs1136659 |
ebi | rs1136659 |
HLI | rs1136659 |
Exac | rs1136659 |
Gnomad | rs1136659 |
Varsome | rs1136659 |
LitVar | rs1136659 |
Map | rs1136659 |
PheGenI | rs1136659 |
Biobank | rs1136659 |
1000 genomes | rs1136659 |
hgdp | rs1136659 |
ensembl | rs1136659 |
geneview | rs1136659 |
scholar | rs1136659 |
rs1136659 | |
pharmgkb | rs1136659 |
gwascentral | rs1136659 |
openSNP | rs1136659 |
23andMe | rs1136659 |
SNPshot | rs1136659 |
SNPdbe | rs1136659 |
MSV3d | rs1136659 |
GWAS Ctlg | rs1136659 |
GMAF | 0.09504 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1136659(A;A) rs1136659(C;C) |
Alt | rs1136659(A;A) rs1136659(C;C) |
Reference | Rs1136659(T;T) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-A |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.29910557T>A; NC_000006.11:g.29910557T>C |
CLNSRC | |
CLNACC |