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

rs151341235

From SNPedia

Merged intors151341233
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341235(G;T)
Make rs151341235(T;T)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324159
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341235
ebirs151341235
HLIrs151341235
Exacrs151341235
Varsomers151341235
Maprs151341235
PheGenIrs151341235
hapmaprs151341235
1000 genomesrs151341235
hgdprs151341235
ensemblrs151341235
gopubmedrs151341235
geneviewrs151341235
scholarrs151341235
googlers151341235
pharmgkbrs151341235
gwascentralrs151341235
openSNPrs151341235
23andMers151341235
23andMe allrs151341235
SNP Nexus

SNPshotrs151341235
SNPdbers151341235
MSV3drs151341235
GWAS Ctlgrs151341235
StatusMerged into rs151341233
Max Magnitude0
ClinVar
Risk rs151341235(T;T)
Alt rs151341235(T;T)
Reference rs151341235(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324159C>A
CLNSRC
CLNACC