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rs12697944

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs12697944(A;A)
Make rs12697944(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356366
GeneHLA-B
is asnp
is mentioned by
dbSNPrs12697944
ebirs12697944
HLIrs12697944
Exacrs12697944
Varsomers12697944
Maprs12697944
PheGenIrs12697944
hapmaprs12697944
1000 genomesrs12697944
hgdprs12697944
ensemblrs12697944
gopubmedrs12697944
geneviewrs12697944
scholarrs12697944
googlers12697944
pharmgkbrs12697944
gwascentralrs12697944
openSNPrs12697944
23andMers12697944
23andMe allrs12697944
SNP Nexus

SNPshotrs12697944
SNPdbers12697944
MSV3drs12697944
GWAS Ctlgrs12697944
Max Magnitude0
ClinVar
Risk rs12697944(A,G,T;A,G,T)
Alt rs12697944(A,G,T;A,G,T)
Reference rs12697944(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324143G>A; NC_000006.11:g.31324143G>C; NC_000006.11:g.31324143G>T
CLNSRC
CLNACC