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rs41548917

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41548917(A;A)
Make rs41548917(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944293
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41548917
ebirs41548917
HLIrs41548917
Exacrs41548917
Varsomers41548917
Maprs41548917
PheGenIrs41548917
hapmaprs41548917
1000 genomesrs41548917
hgdprs41548917
ensemblrs41548917
gopubmedrs41548917
geneviewrs41548917
scholarrs41548917
googlers41548917
pharmgkbrs41548917
gwascentralrs41548917
openSNPrs41548917
23andMers41548917
23andMe allrs41548917
SNP Nexus

SNPshotrs41548917
SNPdbers41548917
MSV3drs41548917
GWAS Ctlgrs41548917
Max Magnitude0
ClinVar
Risk rs41548917(A,T;A,T)
Alt rs41548917(A,T;A,T)
Reference rs41548917(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912070C>A
CLNSRC
CLNACC