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rs139850307

From SNPedia

Merged intors1050556
Orientationminus
Stabilizedplus
Make rs139850307(C;C)
Make rs139850307(C;G)
Make rs139850307(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356809
GeneHLA-B
is asnp
is mentioned by
dbSNPrs139850307
ebirs139850307
HLIrs139850307
Exacrs139850307
Varsomers139850307
Maprs139850307
PheGenIrs139850307
hapmaprs139850307
1000 genomesrs139850307
hgdprs139850307
ensemblrs139850307
gopubmedrs139850307
geneviewrs139850307
scholarrs139850307
googlers139850307
pharmgkbrs139850307
gwascentralrs139850307
openSNPrs139850307
23andMers139850307
23andMe allrs139850307
SNP Nexus

SNPshotrs139850307
SNPdbers139850307
MSV3drs139850307
GWAS Ctlgrs139850307
StatusMerged into rs1050556
Max Magnitude
ClinVar
Risk rs139850307(T;T)
Alt rs139850307(T;T)
Reference rs139850307(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324586C>T
CLNSRC
CLNACC