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rs2916801

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2916801(C;T)
Make rs2916801(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942509
GeneHLA-A
is asnp
is mentioned by
dbSNPrs2916801
ebirs2916801
HLIrs2916801
Exacrs2916801
Varsomers2916801
Maprs2916801
PheGenIrs2916801
hapmaprs2916801
1000 genomesrs2916801
hgdprs2916801
ensemblrs2916801
gopubmedrs2916801
geneviewrs2916801
scholarrs2916801
googlers2916801
pharmgkbrs2916801
gwascentralrs2916801
openSNPrs2916801
23andMers2916801
23andMe allrs2916801
SNP Nexus

SNPshotrs2916801
SNPdbers2916801
MSV3drs2916801
GWAS Ctlgrs2916801
GMAF0.1616
Max Magnitude0
? (C;C) (C;T) (T;T) 28
ClinVar
Risk rs2916801(T;T)
Alt rs2916801(T;T)
Reference rs2916801(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910286C; NC_000006.11:g.29910286C>T
CLNSRC
CLNACC