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rs55965305

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs55965305(C;T)
Make rs55965305(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355562
GeneHLA-B
is asnp
is mentioned by
dbSNPrs55965305
ebirs55965305
HLIrs55965305
Exacrs55965305
Varsomers55965305
Maprs55965305
PheGenIrs55965305
hapmaprs55965305
1000 genomesrs55965305
hgdprs55965305
ensemblrs55965305
gopubmedrs55965305
geneviewrs55965305
scholarrs55965305
googlers55965305
pharmgkbrs55965305
gwascentralrs55965305
openSNPrs55965305
23andMers55965305
23andMe allrs55965305
SNP Nexus

SNPshotrs55965305
SNPdbers55965305
MSV3drs55965305
GWAS Ctlgrs55965305
Max Magnitude0
ClinVar
Risk rs55965305(T;T)
Alt rs55965305(T;T)
Reference rs55965305(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323339G>A
CLNSRC
CLNACC