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rs41556317

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41556317(A;G)
Make rs41556317(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943021
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41556317
ebirs41556317
HLIrs41556317
Exacrs41556317
Varsomers41556317
Maprs41556317
PheGenIrs41556317
hapmaprs41556317
1000 genomesrs41556317
hgdprs41556317
ensemblrs41556317
gopubmedrs41556317
geneviewrs41556317
scholarrs41556317
googlers41556317
pharmgkbrs41556317
gwascentralrs41556317
openSNPrs41556317
23andMers41556317
23andMe allrs41556317
SNP Nexus

SNPshotrs41556317
SNPdbers41556317
MSV3drs41556317
GWAS Ctlgrs41556317
Max Magnitude0
ClinVar
Risk rs41556317(G;G)
Alt rs41556317(G;G)
Reference rs41556317(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910798A>G
CLNSRC
CLNACC