Have questions? Visit https://www.reddit.com/r/SNPedia

rs1131112

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1131112(C;C)
Make rs1131112(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356407
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1131112
ebirs1131112
HLIrs1131112
Exacrs1131112
Varsomers1131112
Maprs1131112
PheGenIrs1131112
hapmaprs1131112
1000 genomesrs1131112
hgdprs1131112
ensemblrs1131112
gopubmedrs1131112
geneviewrs1131112
scholarrs1131112
googlers1131112
pharmgkbrs1131112
gwascentralrs1131112
openSNPrs1131112
23andMers1131112
23andMe allrs1131112
SNP Nexus

SNPshotrs1131112
SNPdbers1131112
MSV3drs1131112
GWAS Ctlgrs1131112
GMAF0.1226
Max Magnitude0
ClinVar
Risk rs1131112(A,C,T;A,C,T)
Alt rs1131112(A,C,T;A,C,T)
Reference rs1131112(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324184C>A; NC_000006.11:g.31324184C>G; NC_000006.11:g.31324184C>T
CLNSRC
CLNACC