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rs2916802

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2916802(C;T)
Make rs2916802(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29945158
GeneHLA-A
is asnp
is mentioned by
dbSNPrs2916802
ebirs2916802
HLIrs2916802
Exacrs2916802
Varsomers2916802
Maprs2916802
PheGenIrs2916802
hapmaprs2916802
1000 genomesrs2916802
hgdprs2916802
ensemblrs2916802
gopubmedrs2916802
geneviewrs2916802
scholarrs2916802
googlers2916802
pharmgkbrs2916802
gwascentralrs2916802
openSNPrs2916802
23andMers2916802
23andMe allrs2916802
SNP Nexus

SNPshotrs2916802
SNPdbers2916802
MSV3drs2916802
GWAS Ctlgrs2916802
Max Magnitude0
ClinVar
Risk rs2916802(T;T)
Alt rs2916802(T;T)
Reference rs2916802(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912935C; NC_000006.11:g.29912935C>T
CLNSRC
CLNACC