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rs41551213

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41551213(C;C)
Make rs41551213(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943392
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41551213
ebirs41551213
HLIrs41551213
Exacrs41551213
Varsomers41551213
Maprs41551213
PheGenIrs41551213
hapmaprs41551213
1000 genomesrs41551213
hgdprs41551213
ensemblrs41551213
gopubmedrs41551213
geneviewrs41551213
scholarrs41551213
googlers41551213
pharmgkbrs41551213
gwascentralrs41551213
openSNPrs41551213
23andMers41551213
23andMe allrs41551213
SNP Nexus

SNPshotrs41551213
SNPdbers41551213
MSV3drs41551213
GWAS Ctlgrs41551213
Max Magnitude0
ClinVar
Risk rs41551213(C,G;C,G)
Alt rs41551213(C,G;C,G)
Reference rs41551213(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911169T>C; NC_000006.11:g.29911169T>G
CLNSRC
CLNACC