rs2523600
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs2523600(C;C) |
Make rs2523600(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31356227 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs2523600 |
dbSNP (classic) | rs2523600 |
ClinGen | rs2523600 |
ebi | rs2523600 |
HLI | rs2523600 |
Exac | rs2523600 |
Gnomad | rs2523600 |
Varsome | rs2523600 |
LitVar | rs2523600 |
Map | rs2523600 |
PheGenI | rs2523600 |
Biobank | rs2523600 |
1000 genomes | rs2523600 |
hgdp | rs2523600 |
ensembl | rs2523600 |
geneview | rs2523600 |
scholar | rs2523600 |
rs2523600 | |
pharmgkb | rs2523600 |
gwascentral | rs2523600 |
openSNP | rs2523600 |
23andMe | rs2523600 |
SNPshot | rs2523600 |
SNPdbe | rs2523600 |
MSV3d | rs2523600 |
GWAS Ctlg | rs2523600 |
GMAF | 0.4766 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs2523600(A;A) rs2523600(C;C) |
Alt | rs2523600(A;A) rs2523600(C;C) |
Reference | Rs2523600(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31324004C>G; NC_000006.11:g.31324004C>T |
CLNSRC | |
CLNACC |