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

rs2276447

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2276447(C;T)
Make rs2276447(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944427
GeneHLA-A
is asnp
is mentioned by
dbSNPrs2276447
dbSNP (old)rs2276447
ClinGenrs2276447
ebirs2276447
HLIrs2276447
Exacrs2276447
Gnomadrs2276447
Varsomers2276447
Maprs2276447
PheGenIrs2276447
Biobankrs2276447
1000 genomesrs2276447
hgdprs2276447
ensemblrs2276447
gopubmedrs2276447
geneviewrs2276447
scholarrs2276447
googlers2276447
pharmgkbrs2276447
gwascentralrs2276447
openSNPrs2276447
23andMers2276447
23andMe allrs2276447
SNP Nexus

SNPshotrs2276447
SNPdbers2276447
MSV3drs2276447
GWAS Ctlgrs2276447
GMAF0.4656
Max Magnitude0
ClinVar
Risk rs2276447(G;G) rs2276447(T;T)
Alt rs2276447(G;G) rs2276447(T;T)
Reference Rs2276447(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912204C>T
CLNSRC
CLNACC