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rs41549012

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41549012(A;G)
Make rs41549012(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943131
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41549012
ebirs41549012
HLIrs41549012
Exacrs41549012
Varsomers41549012
Maprs41549012
PheGenIrs41549012
hapmaprs41549012
1000 genomesrs41549012
hgdprs41549012
ensemblrs41549012
gopubmedrs41549012
geneviewrs41549012
scholarrs41549012
googlers41549012
pharmgkbrs41549012
gwascentralrs41549012
openSNPrs41549012
23andMers41549012
23andMe allrs41549012
SNP Nexus

SNPshotrs41549012
SNPdbers41549012
MSV3drs41549012
GWAS Ctlgrs41549012
Max Magnitude0
ClinVar
Risk rs41549012(G;G)
Alt rs41549012(G;G)
Reference rs41549012(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910908A>G
CLNSRC
CLNACC