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

rs1050683

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1050683(A;A)
Make rs1050683(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356242
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1050683
ebirs1050683
HLIrs1050683
Exacrs1050683
Varsomers1050683
Maprs1050683
PheGenIrs1050683
hapmaprs1050683
1000 genomesrs1050683
hgdprs1050683
ensemblrs1050683
gopubmedrs1050683
geneviewrs1050683
scholarrs1050683
googlers1050683
pharmgkbrs1050683
gwascentralrs1050683
openSNPrs1050683
23andMers1050683
23andMe allrs1050683
SNP Nexus

SNPshotrs1050683
SNPdbers1050683
MSV3drs1050683
GWAS Ctlgrs1050683
Max Magnitude0
ClinVar
Risk rs1050683(A;A)
Alt rs1050683(A;A)
Reference rs1050683(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324019C>T
CLNSRC
CLNACC