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rs41559312

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41559312(A;A)
Make rs41559312(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943320
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41559312
ebirs41559312
HLIrs41559312
Exacrs41559312
Varsomers41559312
Maprs41559312
PheGenIrs41559312
hapmaprs41559312
1000 genomesrs41559312
hgdprs41559312
ensemblrs41559312
gopubmedrs41559312
geneviewrs41559312
scholarrs41559312
googlers41559312
pharmgkbrs41559312
gwascentralrs41559312
openSNPrs41559312
23andMers41559312
23andMe allrs41559312
SNP Nexus

SNPshotrs41559312
SNPdbers41559312
MSV3drs41559312
GWAS Ctlgrs41559312
Max Magnitude0
ClinVar
Risk rs41559312(A;A)
Alt rs41559312(A;A)
Reference rs41559312(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911097C>A
CLNSRC
CLNACC