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rs41561414

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41561414(C;C)
Make rs41561414(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29945124
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41561414
ebirs41561414
HLIrs41561414
Exacrs41561414
Varsomers41561414
Maprs41561414
PheGenIrs41561414
hapmaprs41561414
1000 genomesrs41561414
hgdprs41561414
ensemblrs41561414
gopubmedrs41561414
geneviewrs41561414
scholarrs41561414
googlers41561414
pharmgkbrs41561414
gwascentralrs41561414
openSNPrs41561414
23andMers41561414
23andMe allrs41561414
SNP Nexus

SNPshotrs41561414
SNPdbers41561414
MSV3drs41561414
GWAS Ctlgrs41561414
Max Magnitude0
ClinVar
Risk rs41561414(C;C)
Alt rs41561414(C;C)
Reference rs41561414(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912901T>C
CLNSRC
CLNACC