rs77234140
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs77234140(A;G) |
Make rs77234140(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31356933 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs77234140 |
dbSNP (classic) | rs77234140 |
ClinGen | rs77234140 |
ebi | rs77234140 |
HLI | rs77234140 |
Exac | rs77234140 |
Gnomad | rs77234140 |
Varsome | rs77234140 |
LitVar | rs77234140 |
Map | rs77234140 |
PheGenI | rs77234140 |
Biobank | rs77234140 |
1000 genomes | rs77234140 |
hgdp | rs77234140 |
ensembl | rs77234140 |
geneview | rs77234140 |
scholar | rs77234140 |
rs77234140 | |
pharmgkb | rs77234140 |
gwascentral | rs77234140 |
openSNP | rs77234140 |
23andMe | rs77234140 |
SNPshot | rs77234140 |
SNPdbe | rs77234140 |
MSV3d | rs77234140 |
GWAS Ctlg | rs77234140 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs77234140(C;C) rs77234140(G;G) rs77234140(T;T) |
Alt | rs77234140(C;C) rs77234140(G;G) rs77234140(T;T) |
Reference | Rs77234140(A;A) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31324710T>C |
CLNSRC | |
CLNACC |