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rs151341205

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341205(C;G)
Make rs151341205(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356700
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341205
dbSNP (classic)rs151341205
ClinGenrs151341205
ebirs151341205
HLIrs151341205
Exacrs151341205
Gnomadrs151341205
Varsomers151341205
LitVarrs151341205
Maprs151341205
PheGenIrs151341205
Biobankrs151341205
1000 genomesrs151341205
hgdprs151341205
ensemblrs151341205
geneviewrs151341205
scholarrs151341205
googlers151341205
pharmgkbrs151341205
gwascentralrs151341205
openSNPrs151341205
23andMers151341205
SNPshotrs151341205
SNPdbers151341205
MSV3drs151341205
GWAS Ctlgrs151341205
Max Magnitude0
ClinVar
Risk rs151341205(G;G) rs151341205(T;T)
Alt rs151341205(G;G) rs151341205(T;T)
Reference Rs151341205(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324477G>A; NC_000006.11:g.31324477G>C
CLNSRC
CLNACC