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

rs151341257

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341257(A;A)
Make rs151341257(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356299
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341257
dbSNP (classic)rs151341257
ClinGenrs151341257
ebirs151341257
HLIrs151341257
Exacrs151341257
Gnomadrs151341257
Varsomers151341257
LitVarrs151341257
Maprs151341257
PheGenIrs151341257
Biobankrs151341257
1000 genomesrs151341257
hgdprs151341257
ensemblrs151341257
geneviewrs151341257
scholarrs151341257
googlers151341257
pharmgkbrs151341257
gwascentralrs151341257
openSNPrs151341257
23andMers151341257
SNPshotrs151341257
SNPdbers151341257
MSV3drs151341257
GWAS Ctlgrs151341257
Max Magnitude0
ClinVar
Risk rs151341257(A;A) rs151341257(C;C)
Alt rs151341257(A;A) rs151341257(C;C)
Reference Rs151341257(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324076C>G; NC_000006.11:g.31324076C>T
CLNSRC
CLNACC