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

rs151341242

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151341242(A;G)
Make rs151341242(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356358
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341242
dbSNP (classic)rs151341242
ClinGenrs151341242
ebirs151341242
HLIrs151341242
Exacrs151341242
Gnomadrs151341242
Varsomers151341242
LitVarrs151341242
Maprs151341242
PheGenIrs151341242
Biobankrs151341242
1000 genomesrs151341242
hgdprs151341242
ensemblrs151341242
geneviewrs151341242
scholarrs151341242
googlers151341242
pharmgkbrs151341242
gwascentralrs151341242
openSNPrs151341242
23andMers151341242
SNPshotrs151341242
SNPdbers151341242
MSV3drs151341242
GWAS Ctlgrs151341242
Max Magnitude0
ClinVar
Risk rs151341242(G;G)
Alt rs151341242(G;G)
Reference Rs151341242(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324135T>C
CLNSRC
CLNACC