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rs12721675

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs12721675(A;A)
Make rs12721675(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942827
GeneHLA-A
is asnp
is mentioned by
dbSNPrs12721675
ebirs12721675
HLIrs12721675
Exacrs12721675
Varsomers12721675
Maprs12721675
PheGenIrs12721675
hapmaprs12721675
1000 genomesrs12721675
hgdprs12721675
ensemblrs12721675
gopubmedrs12721675
geneviewrs12721675
scholarrs12721675
googlers12721675
pharmgkbrs12721675
gwascentralrs12721675
openSNPrs12721675
23andMers12721675
23andMe allrs12721675
SNP Nexus

SNPshotrs12721675
SNPdbers12721675
MSV3drs12721675
GWAS Ctlgrs12721675
GMAF0.3577
Max Magnitude0
ClinVar
Risk rs12721675(A,G,T;A,G,T)
Alt rs12721675(A,G,T;A,G,T)
Reference rs12721675(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910604C>A; NC_000006.11:g.29910604C>G; NC_000006.11:g.29910604C>T
CLNSRC
CLNACC