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rs41554614

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41554614(C;T)
Make rs41554614(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942730
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41554614
ebirs41554614
HLIrs41554614
Exacrs41554614
Varsomers41554614
Maprs41554614
PheGenIrs41554614
hapmaprs41554614
1000 genomesrs41554614
hgdprs41554614
ensemblrs41554614
gopubmedrs41554614
geneviewrs41554614
scholarrs41554614
googlers41554614
pharmgkbrs41554614
gwascentralrs41554614
openSNPrs41554614
23andMers41554614
23andMe allrs41554614
SNP Nexus

SNPshotrs41554614
SNPdbers41554614
MSV3drs41554614
GWAS Ctlgrs41554614
Max Magnitude0
ClinVar
Risk rs41554614(T;T)
Alt rs41554614(T;T)
Reference rs41554614(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910507C>T
CLNSRC
CLNACC