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

rs1049645

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1049645(C;T)
Make rs1049645(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354145
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1049645
ebirs1049645
HLIrs1049645
Exacrs1049645
Varsomers1049645
Maprs1049645
PheGenIrs1049645
hapmaprs1049645
1000 genomesrs1049645
hgdprs1049645
ensemblrs1049645
gopubmedrs1049645
geneviewrs1049645
scholarrs1049645
googlers1049645
pharmgkbrs1049645
gwascentralrs1049645
openSNPrs1049645
23andMers1049645
23andMe allrs1049645
SNP Nexus

SNPshotrs1049645
SNPdbers1049645
MSV3drs1049645
GWAS Ctlgrs1049645
GMAF0.01102
Max Magnitude0
ClinVar
Risk rs1049645(T;T)
Alt rs1049645(T;T)
Reference rs1049645(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31321922G>A
CLNSRC
CLNACC