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rs41562919

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41562919(A;A)
Make rs41562919(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944207
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41562919
ebirs41562919
HLIrs41562919
Exacrs41562919
Varsomers41562919
Maprs41562919
PheGenIrs41562919
hapmaprs41562919
1000 genomesrs41562919
hgdprs41562919
ensemblrs41562919
gopubmedrs41562919
geneviewrs41562919
scholarrs41562919
googlers41562919
pharmgkbrs41562919
gwascentralrs41562919
openSNPrs41562919
23andMers41562919
23andMe allrs41562919
SNP Nexus

SNPshotrs41562919
SNPdbers41562919
MSV3drs41562919
GWAS Ctlgrs41562919
Max Magnitude0
ClinVar
Risk rs41562919(A;A)
Alt rs41562919(A;A)
Reference rs41562919(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911984G>A
CLNSRC
CLNACC