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rs41559916

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41559916(A;A)
Make rs41559916(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943519
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41559916
ebirs41559916
HLIrs41559916
Exacrs41559916
Varsomers41559916
Maprs41559916
PheGenIrs41559916
hapmaprs41559916
1000 genomesrs41559916
hgdprs41559916
ensemblrs41559916
gopubmedrs41559916
geneviewrs41559916
scholarrs41559916
googlers41559916
pharmgkbrs41559916
gwascentralrs41559916
openSNPrs41559916
23andMers41559916
23andMe allrs41559916
SNP Nexus

SNPshotrs41559916
SNPdbers41559916
MSV3drs41559916
GWAS Ctlgrs41559916
GMAF0.1414
Max Magnitude0
ClinVar
Risk rs41559916(A,C,T;A,C,T)
Alt rs41559916(A,C,T;A,C,T)
Reference rs41559916(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911296G>A; NC_000006.11:g.29911296G>C; NC_000006.11:g.29911296G>T
CLNSRC
CLNACC