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rs12697943

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs12697943(G;T)
Make rs12697943(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356280
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs12697943
dbSNP (classic)rs12697943
ClinGenrs12697943
ebirs12697943
HLIrs12697943
Exacrs12697943
Gnomadrs12697943
Varsomers12697943
LitVarrs12697943
Maprs12697943
PheGenIrs12697943
Biobankrs12697943
1000 genomesrs12697943
hgdprs12697943
ensemblrs12697943
geneviewrs12697943
scholarrs12697943
googlers12697943
pharmgkbrs12697943
gwascentralrs12697943
openSNPrs12697943
23andMers12697943
SNPshotrs12697943
SNPdbers12697943
MSV3drs12697943
GWAS Ctlgrs12697943
Max Magnitude0
ClinVar
Risk rs12697943(A;A) rs12697943(C;C) rs12697943(T;T)
Alt rs12697943(A;A) rs12697943(C;C) rs12697943(T;T)
Reference Rs12697943(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324057C>A; NC_000006.11:g.31324057C>G; NC_000006.11:g.31324057C>T
CLNSRC
CLNACC