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rs151341260

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341260(-;-)
Make rs151341260(-;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324072
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341260
dbSNP (classic)rs151341260
ClinGenrs151341260
ebirs151341260
HLIrs151341260
Exacrs151341260
Gnomadrs151341260
Varsomers151341260
LitVarrs151341260
Maprs151341260
PheGenIrs151341260
Biobankrs151341260
1000 genomesrs151341260
hgdprs151341260
ensemblrs151341260
geneviewrs151341260
scholarrs151341260
googlers151341260
pharmgkbrs151341260
gwascentralrs151341260
openSNPrs151341260
23andMers151341260
SNPshotrs151341260
SNPdbers151341260
MSV3drs151341260
GWAS Ctlgrs151341260
StatusDeleted
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs151341260(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324072delG
CLNSRC
CLNACC