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rs151341165

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341165(C;G)
Make rs151341165(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356776
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341165
ebirs151341165
HLIrs151341165
Exacrs151341165
Varsomers151341165
Maprs151341165
PheGenIrs151341165
hapmaprs151341165
1000 genomesrs151341165
hgdprs151341165
ensemblrs151341165
gopubmedrs151341165
geneviewrs151341165
scholarrs151341165
googlers151341165
pharmgkbrs151341165
gwascentralrs151341165
openSNPrs151341165
23andMers151341165
23andMe allrs151341165
SNP Nexus

SNPshotrs151341165
SNPdbers151341165
MSV3drs151341165
GWAS Ctlgrs151341165
Merged fromRs151341166
Max Magnitude0
ClinVar
Risk rs151341165(A,G;A,G)
Alt rs151341165(A,G;A,G)
Reference rs151341165(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324553G>C; NC_000006.11:g.31324553G>T
CLNSRC
CLNACC