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rs12721717

From SNPedia

Merged intors1059498
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs12721717(C;C)
Make rs12721717(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943338
GeneHLA-A
is asnp
is mentioned by
dbSNPrs12721717
dbSNP (classic)rs12721717
ClinGenrs12721717
ebirs12721717
HLIrs12721717
Exacrs12721717
Gnomadrs12721717
Varsomers12721717
LitVarrs12721717
Maprs12721717
PheGenIrs12721717
Biobankrs12721717
1000 genomesrs12721717
hgdprs12721717
ensemblrs12721717
geneviewrs12721717
scholarrs12721717
googlers12721717
pharmgkbrs12721717
gwascentralrs12721717
openSNPrs12721717
23andMers12721717
SNPshotrs12721717
SNPdbers12721717
MSV3drs12721717
GWAS Ctlgrs12721717
StatusMerged into rs1059498
GMAF0.432
Max Magnitude0
ClinVar
Risk rs12721717(A;A) rs12721717(C;C) rs12721717(T;T)
Alt rs12721717(A;A) rs12721717(C;C) rs12721717(T;T)
Reference Rs12721717(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911115G>A; NC_000006.11:g.29911115G>C; NC_000006.11:g.29911115G>T
CLNSRC
CLNACC