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rs66473235

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs66473235(-;-)
Make rs66473235(-;A)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356721
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs66473235
dbSNP (classic)rs66473235
ClinGenrs66473235
ebirs66473235
HLIrs66473235
Exacrs66473235
Gnomadrs66473235
Varsomers66473235
LitVarrs66473235
Maprs66473235
PheGenIrs66473235
Biobankrs66473235
1000 genomesrs66473235
hgdprs66473235
ensemblrs66473235
geneviewrs66473235
scholarrs66473235
googlers66473235
pharmgkbrs66473235
gwascentralrs66473235
openSNPrs66473235
23andMers66473235
SNPshotrs66473235
SNPdbers66473235
MSV3drs66473235
GWAS Ctlgrs66473235
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs66473235(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324498delT
CLNSRC
CLNACC