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

rs1050570

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
(AA;AA) 0 common in clinvar
Make rs1050570(A;G)
Make rs1050570(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356772
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs1050570
dbSNP (classic)rs1050570
ClinGenrs1050570
ebirs1050570
HLIrs1050570
Exacrs1050570
Gnomadrs1050570
Varsomers1050570
LitVarrs1050570
Maprs1050570
PheGenIrs1050570
Biobankrs1050570
1000 genomesrs1050570
hgdprs1050570
ensemblrs1050570
geneviewrs1050570
scholarrs1050570
googlers1050570
pharmgkbrs1050570
gwascentralrs1050570
openSNPrs1050570
23andMers1050570
SNPshotrs1050570
SNPdbers1050570
MSV3drs1050570
GWAS Ctlgrs1050570
GMAF0.3503
Max Magnitude0
ClinVar
Risk rs1050570(G;G)
Alt rs1050570(G;G)
Reference Rs1050570(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324549T>C
CLNSRC
CLNACC