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

rs151341210

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs151341210(-;CCC)
Make rs151341210(CCC;CCC)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324430
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341210
dbSNP (classic)rs151341210
ClinGenrs151341210
ebirs151341210
HLIrs151341210
Exacrs151341210
Gnomadrs151341210
Varsomers151341210
LitVarrs151341210
Maprs151341210
PheGenIrs151341210
Biobankrs151341210
1000 genomesrs151341210
hgdprs151341210
ensemblrs151341210
geneviewrs151341210
scholarrs151341210
googlers151341210
pharmgkbrs151341210
gwascentralrs151341210
openSNPrs151341210
23andMers151341210
SNPshotrs151341210
SNPdbers151341210
MSV3drs151341210
GWAS Ctlgrs151341210
StatusDeleted
Max Magnitude0
ClinVar
Risk rs151341210(CCC;CCC)
Alt rs151341210(CCC;CCC)
Reference Rs151341210(;)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324430_31324431insGGG
CLNSRC
CLNACC