Have questions? Visit https://www.reddit.com/r/SNPedia

rs78135486

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs78135486(A;A)
Make rs78135486(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355552
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs78135486
dbSNP (classic)rs78135486
ClinGenrs78135486
ebirs78135486
HLIrs78135486
Exacrs78135486
Gnomadrs78135486
Varsomers78135486
LitVarrs78135486
Maprs78135486
PheGenIrs78135486
Biobankrs78135486
1000 genomesrs78135486
hgdprs78135486
ensemblrs78135486
geneviewrs78135486
scholarrs78135486
googlers78135486
pharmgkbrs78135486
gwascentralrs78135486
openSNPrs78135486
23andMers78135486
SNPshotrs78135486
SNPdbers78135486
MSV3drs78135486
GWAS Ctlgrs78135486
Max Magnitude0
ClinVar
Risk rs78135486(A;A)
Alt rs78135486(A;A)
Reference Rs78135486(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323329G>T
CLNSRC
CLNACC