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rs41548122

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41548122(-;-)
Make rs41548122(-;T)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position29911074
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41548122
ebirs41548122
HLIrs41548122
Exacrs41548122
Varsomers41548122
Maprs41548122
PheGenIrs41548122
hapmaprs41548122
1000 genomesrs41548122
hgdprs41548122
ensemblrs41548122
gopubmedrs41548122
geneviewrs41548122
scholarrs41548122
googlers41548122
pharmgkbrs41548122
gwascentralrs41548122
openSNPrs41548122
23andMers41548122
23andMe allrs41548122
SNP Nexus

SNPshotrs41548122
SNPdbers41548122
MSV3drs41548122
GWAS Ctlgrs41548122
StatusDeleted
Max Magnitude0
ClinVar
Risk rs41548122(;)
Alt rs41548122(;)
Reference rs41548122(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911074delT
CLNSRC
CLNACC