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rs151341395

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs151341395(G;G)
Make rs151341395(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354676
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341395
ClinGenrs151341395
ebirs151341395
HLIrs151341395
Exacrs151341395
Varsomers151341395
Maprs151341395
PheGenIrs151341395
hapmaprs151341395
1000 genomesrs151341395
hgdprs151341395
ensemblrs151341395
gopubmedrs151341395
geneviewrs151341395
scholarrs151341395
googlers151341395
pharmgkbrs151341395
gwascentralrs151341395
openSNPrs151341395
23andMers151341395
23andMe allrs151341395
SNP Nexus

SNPshotrs151341395
SNPdbers151341395
MSV3drs151341395
GWAS Ctlgrs151341395
Max Magnitude0
ClinVar
Risk rs151341395(G;G)
Alt rs151341395(G;G)
Reference Rs151341395(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322453A>C
CLNSRC
CLNACC


[ea77323f08dccd84013ea888] 2017-07-25 05:04:08: Fatal exception of type "DBConnectionError"