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rs76388977

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs76388977(A;A)
Make rs76388977(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944347
GeneHLA-A
is asnp
is mentioned by
dbSNPrs76388977
ebirs76388977
HLIrs76388977
Exacrs76388977
Varsomers76388977
Maprs76388977
PheGenIrs76388977
hapmaprs76388977
1000 genomesrs76388977
hgdprs76388977
ensemblrs76388977
gopubmedrs76388977
geneviewrs76388977
scholarrs76388977
googlers76388977
pharmgkbrs76388977
gwascentralrs76388977
openSNPrs76388977
23andMers76388977
23andMe allrs76388977
SNP Nexus

SNPshotrs76388977
SNPdbers76388977
MSV3drs76388977
GWAS Ctlgrs76388977
Max Magnitude0
ClinVar
Risk rs76388977(A;A)
Alt rs76388977(A;A)
Reference rs76388977(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912124C>A
CLNSRC
CLNACC