Have questions? Visit https://www.reddit.com/r/SNPedia

rs709054

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs709054(C;G)
Make rs709054(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356309
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs709054
dbSNP (classic)rs709054
ClinGenrs709054
ebirs709054
HLIrs709054
Exacrs709054
Gnomadrs709054
Varsomers709054
LitVarrs709054
Maprs709054
PheGenIrs709054
Biobankrs709054
1000 genomesrs709054
hgdprs709054
ensemblrs709054
geneviewrs709054
scholarrs709054
googlers709054
pharmgkbrs709054
gwascentralrs709054
openSNPrs709054
23andMers709054
SNPshotrs709054
SNPdbers709054
MSV3drs709054
GWAS Ctlgrs709054
GMAF0.4646
Max Magnitude0
ClinVar
Risk rs709054(A;A) rs709054(G;G) rs709054(T;T)
Alt rs709054(A;A) rs709054(G;G) rs709054(T;T)
Reference Rs709054(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324086G>C; NC_000006.11:g.31324086G>T
CLNSRC
CLNACC