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rs77234140

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs77234140(A;G)
Make rs77234140(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356933
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs77234140
dbSNP (classic)rs77234140
ClinGenrs77234140
ebirs77234140
HLIrs77234140
Exacrs77234140
Gnomadrs77234140
Varsomers77234140
LitVarrs77234140
Maprs77234140
PheGenIrs77234140
Biobankrs77234140
1000 genomesrs77234140
hgdprs77234140
ensemblrs77234140
geneviewrs77234140
scholarrs77234140
googlers77234140
pharmgkbrs77234140
gwascentralrs77234140
openSNPrs77234140
23andMers77234140
SNPshotrs77234140
SNPdbers77234140
MSV3drs77234140
GWAS Ctlgrs77234140
Max Magnitude0
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