rs1065378
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs1065378(A;C) |
Make rs1065378(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31356856 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs1065378 |
dbSNP (classic) | rs1065378 |
ClinGen | rs1065378 |
ebi | rs1065378 |
HLI | rs1065378 |
Exac | rs1065378 |
Gnomad | rs1065378 |
Varsome | rs1065378 |
LitVar | rs1065378 |
Map | rs1065378 |
PheGenI | rs1065378 |
Biobank | rs1065378 |
1000 genomes | rs1065378 |
hgdp | rs1065378 |
ensembl | rs1065378 |
geneview | rs1065378 |
scholar | rs1065378 |
rs1065378 | |
pharmgkb | rs1065378 |
gwascentral | rs1065378 |
openSNP | rs1065378 |
23andMe | rs1065378 |
SNPshot | rs1065378 |
SNPdbe | rs1065378 |
MSV3d | rs1065378 |
GWAS Ctlg | rs1065378 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1065378(C;C) rs1065378(G;G) |
Alt | rs1065378(C;C) rs1065378(G;G) |
Reference | Rs1065378(A;A) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31324633T>C; NC_000006.11:g.31324633T>G |
CLNSRC | |
CLNACC |