rs142964417
From SNPedia
Merged into | rs1050370 |
Orientation | minus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs142964417(A;A) |
Make rs142964417(A;C) |
Make rs142964417(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31356312 |
Gene | HLA-B |
is a | snp |
is | mentioned by |
dbSNP | rs142964417 |
dbSNP (classic) | rs142964417 |
ClinGen | rs142964417 |
ebi | rs142964417 |
HLI | rs142964417 |
Exac | rs142964417 |
Gnomad | rs142964417 |
Varsome | rs142964417 |
LitVar | rs142964417 |
Map | rs142964417 |
PheGenI | rs142964417 |
Biobank | rs142964417 |
1000 genomes | rs142964417 |
hgdp | rs142964417 |
ensembl | rs142964417 |
geneview | rs142964417 |
scholar | rs142964417 |
rs142964417 | |
pharmgkb | rs142964417 |
gwascentral | rs142964417 |
openSNP | rs142964417 |
23andMe | rs142964417 |
SNPshot | rs142964417 |
SNPdbe | rs142964417 |
MSV3d | rs142964417 |
GWAS Ctlg | rs142964417 |
Status | Merged into rs1050370 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs142964417(A;A) |
Alt | rs142964417(A;A) |
Reference | Rs142964417(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.31324089G>A |
CLNSRC | |
CLNACC |