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rs41562119

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41562119(C;G)
Make rs41562119(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943007
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41562119
ebirs41562119
HLIrs41562119
Exacrs41562119
Varsomers41562119
Maprs41562119
PheGenIrs41562119
hapmaprs41562119
1000 genomesrs41562119
hgdprs41562119
ensemblrs41562119
gopubmedrs41562119
geneviewrs41562119
scholarrs41562119
googlers41562119
pharmgkbrs41562119
gwascentralrs41562119
openSNPrs41562119
23andMers41562119
23andMe allrs41562119
SNP Nexus

SNPshotrs41562119
SNPdbers41562119
MSV3drs41562119
GWAS Ctlgrs41562119
Max Magnitude0
ClinVar
Risk rs41562119(G,T;G,T)
Alt rs41562119(G,T;G,T)
Reference rs41562119(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910784C>G; NC_000006.11:g.29910784C>T
CLNSRC
CLNACC