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rs7768403

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs7768403(C;T)
Make rs7768403(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354989
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs7768403
dbSNP (classic)rs7768403
ClinGenrs7768403
ebirs7768403
HLIrs7768403
Exacrs7768403
Gnomadrs7768403
Varsomers7768403
LitVarrs7768403
Maprs7768403
PheGenIrs7768403
Biobankrs7768403
1000 genomesrs7768403
hgdprs7768403
ensemblrs7768403
geneviewrs7768403
scholarrs7768403
googlers7768403
pharmgkbrs7768403
gwascentralrs7768403
openSNPrs7768403
23andMers7768403
SNPshotrs7768403
SNPdbers7768403
MSV3drs7768403
GWAS Ctlgrs7768403
GMAF0.01102
Max Magnitude0
ClinVar
Risk rs7768403(T;T)
Alt rs7768403(T;T)
Reference Rs7768403(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31322766C>T
CLNSRC
CLNACC