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rs70990234

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs70990234(-;GAAGGGCTCCA)
Make rs70990234(GAAGGGCTCCA;GAAGGGCTCCA)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355262
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs70990234
dbSNP (classic)rs70990234
ClinGenrs70990234
ebirs70990234
HLIrs70990234
Exacrs70990234
Gnomadrs70990234
Varsomers70990234
LitVarrs70990234
Maprs70990234
PheGenIrs70990234
Biobankrs70990234
1000 genomesrs70990234
hgdprs70990234
ensemblrs70990234
geneviewrs70990234
scholarrs70990234
googlers70990234
pharmgkbrs70990234
gwascentralrs70990234
openSNPrs70990234
23andMers70990234
SNPshotrs70990234
SNPdbers70990234
MSV3drs70990234
GWAS Ctlgrs70990234
GMAF0.461
Max Magnitude0
ClinVar
Risk rs70990234(GAAGGGCTCCA;GAAGGGCTCCA)
Alt rs70990234(GAAGGGCTCCA;GAAGGGCTCCA)
Reference Rs70990234(;)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31323039_31323040insGAAGGGCTCCA
CLNSRC
CLNACC