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rs41542119

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41542119(C;C)
Make rs41542119(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943369
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41542119
ebirs41542119
HLIrs41542119
Exacrs41542119
Varsomers41542119
Maprs41542119
PheGenIrs41542119
hapmaprs41542119
1000 genomesrs41542119
hgdprs41542119
ensemblrs41542119
gopubmedrs41542119
geneviewrs41542119
scholarrs41542119
googlers41542119
pharmgkbrs41542119
gwascentralrs41542119
openSNPrs41542119
23andMers41542119
23andMe allrs41542119
SNP Nexus

SNPshotrs41542119
SNPdbers41542119
MSV3drs41542119
GWAS Ctlgrs41542119
Max Magnitude0
ClinVar
Risk rs41542119(A,C,T;A,C,T)
Alt rs41542119(A,C,T;A,C,T)
Reference rs41542119(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911146G>A; NC_000006.11:g.29911146G>C; NC_000006.11:g.29911146G>T
CLNSRC
CLNACC