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rs41549215

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41549215(C;C)
Make rs41549215(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942843
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41549215
ebirs41549215
HLIrs41549215
Exacrs41549215
Varsomers41549215
Maprs41549215
PheGenIrs41549215
hapmaprs41549215
1000 genomesrs41549215
hgdprs41549215
ensemblrs41549215
gopubmedrs41549215
geneviewrs41549215
scholarrs41549215
googlers41549215
pharmgkbrs41549215
gwascentralrs41549215
openSNPrs41549215
23andMers41549215
23andMe allrs41549215
SNP Nexus

SNPshotrs41549215
SNPdbers41549215
MSV3drs41549215
GWAS Ctlgrs41549215
Max Magnitude0
ClinVar
Risk rs41549215(A,C,T;A,C,T)
Alt rs41549215(A,C,T;A,C,T)
Reference rs41549215(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910620G>A; NC_000006.11:g.29910620G>C; NC_000006.11:g.29910620G>T
CLNSRC
CLNACC