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rs114818671

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs114818671(C;C)
Make rs114818671(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944372
GeneHLA-A
is asnp
is mentioned by
dbSNPrs114818671
ebirs114818671
HLIrs114818671
Exacrs114818671
Varsomers114818671
Maprs114818671
PheGenIrs114818671
hapmaprs114818671
1000 genomesrs114818671
hgdprs114818671
ensemblrs114818671
gopubmedrs114818671
geneviewrs114818671
scholarrs114818671
googlers114818671
pharmgkbrs114818671
gwascentralrs114818671
openSNPrs114818671
23andMers114818671
23andMe allrs114818671
SNP Nexus

SNPshotrs114818671
SNPdbers114818671
MSV3drs114818671
GWAS Ctlgrs114818671
GMAF0.06979
Max Magnitude0
ClinVar
Risk rs114818671(C;C)
Alt rs114818671(C;C)
Reference rs114818671(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912149G>C
CLNSRC
CLNACC