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rs41562412

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41562412(A;A)
Make rs41562412(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942899
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41562412
ebirs41562412
HLIrs41562412
Exacrs41562412
Varsomers41562412
Maprs41562412
PheGenIrs41562412
hapmaprs41562412
1000 genomesrs41562412
hgdprs41562412
ensemblrs41562412
gopubmedrs41562412
geneviewrs41562412
scholarrs41562412
googlers41562412
pharmgkbrs41562412
gwascentralrs41562412
openSNPrs41562412
23andMers41562412
23andMe allrs41562412
SNP Nexus

SNPshotrs41562412
SNPdbers41562412
MSV3drs41562412
GWAS Ctlgrs41562412
Max Magnitude0
ClinVar
Risk rs41562412(A,T;A,T)
Alt rs41562412(A,T;A,T)
Reference rs41562412(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910676G>A; NC_000006.11:g.29910676G>T
CLNSRC
CLNACC