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

rs1055849

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1055849(C;C)
Make rs1055849(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354139
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1055849
ebirs1055849
HLIrs1055849
Exacrs1055849
Varsomers1055849
Maprs1055849
PheGenIrs1055849
hapmaprs1055849
1000 genomesrs1055849
hgdprs1055849
ensemblrs1055849
gopubmedrs1055849
geneviewrs1055849
scholarrs1055849
googlers1055849
pharmgkbrs1055849
gwascentralrs1055849
openSNPrs1055849
23andMers1055849
23andMe allrs1055849
SNP Nexus

SNPshotrs1055849
SNPdbers1055849
MSV3drs1055849
GWAS Ctlgrs1055849
GMAF0.2856
Max Magnitude0
ClinVar
Risk rs1055849(C,G;C,G)
Alt rs1055849(C,G;C,G)
Reference rs1055849(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31321916A>C; NC_000006.11:g.31321916A>G
CLNSRC
CLNACC