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rs41562020

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41562020(C;T)
Make rs41562020(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942784
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41562020
ebirs41562020
HLIrs41562020
Exacrs41562020
Varsomers41562020
Maprs41562020
PheGenIrs41562020
hapmaprs41562020
1000 genomesrs41562020
hgdprs41562020
ensemblrs41562020
gopubmedrs41562020
geneviewrs41562020
scholarrs41562020
googlers41562020
pharmgkbrs41562020
gwascentralrs41562020
openSNPrs41562020
23andMers41562020
23andMe allrs41562020
SNP Nexus

SNPshotrs41562020
SNPdbers41562020
MSV3drs41562020
GWAS Ctlgrs41562020
Max Magnitude0
ClinVar
Risk rs41562020(T;T)
Alt rs41562020(T;T)
Reference rs41562020(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910561C>T
CLNSRC
CLNACC