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rs697742

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs697742(G;T)
Make rs697742(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356247
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs697742
dbSNP (old)rs697742
ClinGenrs697742
ebirs697742
HLIrs697742
Exacrs697742
Gnomadrs697742
Varsomers697742
Maprs697742
PheGenIrs697742
Biobankrs697742
1000 genomesrs697742
hgdprs697742
ensemblrs697742
gopubmedrs697742
geneviewrs697742
scholarrs697742
googlers697742
pharmgkbrs697742
gwascentralrs697742
openSNPrs697742
23andMers697742
23andMe allrs697742
SNP Nexus

SNPshotrs697742
SNPdbers697742
MSV3drs697742
GWAS Ctlgrs697742
GMAF0.4798
Max Magnitude0
ClinVar
Risk rs697742(A;A) rs697742(T;T)
Alt rs697742(A;A) rs697742(T;T)
Reference Rs697742(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324024C>A; NC_000006.11:g.31324024C>T
CLNSRC
CLNACC