rs1055849
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs1055849(C;C) |
Make rs1055849(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31354139 |
Gene | HLA-B |
is a | snp |
is | mentioned by |
dbSNP | rs1055849 |
dbSNP (classic) | rs1055849 |
ClinGen | rs1055849 |
ebi | rs1055849 |
HLI | rs1055849 |
Exac | rs1055849 |
Gnomad | rs1055849 |
Varsome | rs1055849 |
LitVar | rs1055849 |
Map | rs1055849 |
PheGenI | rs1055849 |
Biobank | rs1055849 |
1000 genomes | rs1055849 |
hgdp | rs1055849 |
ensembl | rs1055849 |
geneview | rs1055849 |
scholar | rs1055849 |
rs1055849 | |
pharmgkb | rs1055849 |
gwascentral | rs1055849 |
openSNP | rs1055849 |
23andMe | rs1055849 |
SNPshot | rs1055849 |
SNPdbe | rs1055849 |
MSV3d | rs1055849 |
GWAS Ctlg | rs1055849 |
GMAF | 0.2856 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1055849(C;C) rs1055849(G;G) |
Alt | rs1055849(C;C) rs1055849(G;G) |
Reference | Rs1055849(T;T) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31321916A>C; NC_000006.11:g.31321916A>G |
CLNSRC | |
CLNACC |