rs1131235
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs1131235(A;A) |
Make rs1131235(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31356429 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs1131235 |
dbSNP (classic) | rs1131235 |
ClinGen | rs1131235 |
ebi | rs1131235 |
HLI | rs1131235 |
Exac | rs1131235 |
Gnomad | rs1131235 |
Varsome | rs1131235 |
LitVar | rs1131235 |
Map | rs1131235 |
PheGenI | rs1131235 |
Biobank | rs1131235 |
1000 genomes | rs1131235 |
hgdp | rs1131235 |
ensembl | rs1131235 |
geneview | rs1131235 |
scholar | rs1131235 |
rs1131235 | |
pharmgkb | rs1131235 |
gwascentral | rs1131235 |
openSNP | rs1131235 |
23andMe | rs1131235 |
SNPshot | rs1131235 |
SNPdbe | rs1131235 |
MSV3d | rs1131235 |
GWAS Ctlg | rs1131235 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1131235(A;A) rs1131235(G;G) rs1131235(T;T) |
Alt | rs1131235(A;A) rs1131235(G;G) rs1131235(T;T) |
Reference | Rs1131235(C;C) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31324206G>A; NC_000006.11:g.31324206G>C; NC_000006.11:g.31324206G>T |
CLNSRC | |
CLNACC |