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rs41544717

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41544717(C;T)
Make rs41544717(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944123
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41544717
ebirs41544717
HLIrs41544717
Exacrs41544717
Varsomers41544717
Maprs41544717
PheGenIrs41544717
hapmaprs41544717
1000 genomesrs41544717
hgdprs41544717
ensemblrs41544717
gopubmedrs41544717
geneviewrs41544717
scholarrs41544717
googlers41544717
pharmgkbrs41544717
gwascentralrs41544717
openSNPrs41544717
23andMers41544717
23andMe allrs41544717
SNP Nexus

SNPshotrs41544717
SNPdbers41544717
MSV3drs41544717
GWAS Ctlgrs41544717
Max Magnitude0
ClinVar
Risk rs41544717(T;T)
Alt rs41544717(T;T)
Reference rs41544717(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911900C>T
CLNSRC
CLNACC