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rs76385482

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs76385482(A;A)
Make rs76385482(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943399
GeneHLA-A
is asnp
is mentioned by
dbSNPrs76385482
ebirs76385482
HLIrs76385482
Exacrs76385482
Varsomers76385482
Maprs76385482
PheGenIrs76385482
hapmaprs76385482
1000 genomesrs76385482
hgdprs76385482
ensemblrs76385482
gopubmedrs76385482
geneviewrs76385482
scholarrs76385482
googlers76385482
pharmgkbrs76385482
gwascentralrs76385482
openSNPrs76385482
23andMers76385482
23andMe allrs76385482
SNP Nexus

SNPshotrs76385482
SNPdbers76385482
MSV3drs76385482
GWAS Ctlgrs76385482
Max Magnitude0
ClinVar
Risk rs76385482(A,C,T;A,C,T)
Alt rs76385482(A,C,T;A,C,T)
Reference rs76385482(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911176G>A; NC_000006.11:g.29911176G>C; NC_000006.11:g.29911176G>T
CLNSRC
CLNACC