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rs2916803

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs2916803(C;C)
Make rs2916803(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29945167
GeneHLA-A
is asnp
is mentioned by
dbSNPrs2916803
ebirs2916803
HLIrs2916803
Exacrs2916803
Varsomers2916803
Maprs2916803
PheGenIrs2916803
hapmaprs2916803
1000 genomesrs2916803
hgdprs2916803
ensemblrs2916803
gopubmedrs2916803
geneviewrs2916803
scholarrs2916803
googlers2916803
pharmgkbrs2916803
gwascentralrs2916803
openSNPrs2916803
23andMers2916803
23andMe allrs2916803
SNP Nexus

SNPshotrs2916803
SNPdbers2916803
MSV3drs2916803
GWAS Ctlgrs2916803
GMAF0.1465
Max Magnitude0
ClinVar
Risk rs2916803(C;C)
Alt rs2916803(C;C)
Reference rs2916803(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912944T; NC_000006.11:g.29912944T>C
CLNSRC
CLNACC