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rs41562118

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41562118(A;A)
Make rs41562118(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943447
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41562118
ebirs41562118
HLIrs41562118
Exacrs41562118
Varsomers41562118
Maprs41562118
PheGenIrs41562118
hapmaprs41562118
1000 genomesrs41562118
hgdprs41562118
ensemblrs41562118
gopubmedrs41562118
geneviewrs41562118
scholarrs41562118
googlers41562118
pharmgkbrs41562118
gwascentralrs41562118
openSNPrs41562118
23andMers41562118
23andMe allrs41562118
SNP Nexus

SNPshotrs41562118
SNPdbers41562118
MSV3drs41562118
GWAS Ctlgrs41562118
Max Magnitude0
ClinVar
Risk rs41562118(A,G,T;A,G,T)
Alt rs41562118(A,G,T;A,G,T)
Reference rs41562118(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911224C>A; NC_000006.11:g.29911224C>G; NC_000006.11:g.29911224C>T
CLNSRC
CLNACC