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

rs75202290

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs75202290(A;A)
Make rs75202290(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356236
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs75202290
dbSNP (classic)rs75202290
ClinGenrs75202290
ebirs75202290
HLIrs75202290
Exacrs75202290
Gnomadrs75202290
Varsomers75202290
LitVarrs75202290
Maprs75202290
PheGenIrs75202290
Biobankrs75202290
1000 genomesrs75202290
hgdprs75202290
ensemblrs75202290
geneviewrs75202290
scholarrs75202290
googlers75202290
pharmgkbrs75202290
gwascentralrs75202290
openSNPrs75202290
23andMers75202290
SNPshotrs75202290
SNPdbers75202290
MSV3drs75202290
GWAS Ctlgrs75202290
Max Magnitude0
ClinVar
Risk rs75202290(A;A) rs75202290(T;T)
Alt rs75202290(A;A) rs75202290(T;T)
Reference Rs75202290(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324013G>A; NC_000006.11:g.31324013G>T
CLNSRC
CLNACC