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rs151341181

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341181(-;-)
Make rs151341181(-;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324545
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341181
dbSNP (classic)rs151341181
ClinGenrs151341181
ebirs151341181
HLIrs151341181
Exacrs151341181
Gnomadrs151341181
Varsomers151341181
LitVarrs151341181
Maprs151341181
PheGenIrs151341181
Biobankrs151341181
1000 genomesrs151341181
hgdprs151341181
ensemblrs151341181
geneviewrs151341181
scholarrs151341181
googlers151341181
pharmgkbrs151341181
gwascentralrs151341181
openSNPrs151341181
23andMers151341181
SNPshotrs151341181
SNPdbers151341181
MSV3drs151341181
GWAS Ctlgrs151341181
StatusDeleted
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs151341181(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324545delG
CLNSRC
CLNACC