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rs41562213

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41562213(C;T)
Make rs41562213(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943234
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41562213
ebirs41562213
HLIrs41562213
Exacrs41562213
Varsomers41562213
Maprs41562213
PheGenIrs41562213
hapmaprs41562213
1000 genomesrs41562213
hgdprs41562213
ensemblrs41562213
gopubmedrs41562213
geneviewrs41562213
scholarrs41562213
googlers41562213
pharmgkbrs41562213
gwascentralrs41562213
openSNPrs41562213
23andMers41562213
23andMe allrs41562213
SNP Nexus

SNPshotrs41562213
SNPdbers41562213
MSV3drs41562213
GWAS Ctlgrs41562213
GMAF0.0877
Max Magnitude0
ClinVar
Risk rs41562213(T;T)
Alt rs41562213(T;T)
Reference rs41562213(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911011C>T
CLNSRC
CLNACC