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rs41561719

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41561719(A;A)
Make rs41561719(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943319
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41561719
ebirs41561719
HLIrs41561719
Exacrs41561719
Varsomers41561719
Maprs41561719
PheGenIrs41561719
hapmaprs41561719
1000 genomesrs41561719
hgdprs41561719
ensemblrs41561719
gopubmedrs41561719
geneviewrs41561719
scholarrs41561719
googlers41561719
pharmgkbrs41561719
gwascentralrs41561719
openSNPrs41561719
23andMers41561719
23andMe allrs41561719
SNP Nexus

SNPshotrs41561719
SNPdbers41561719
MSV3drs41561719
GWAS Ctlgrs41561719
Max Magnitude0
ClinVar
Risk rs41561719(A,C,T;A,C,T)
Alt rs41561719(A,C,T;A,C,T)
Reference rs41561719(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911096G>A; NC_000006.11:g.29911096G>C; NC_000006.11:g.29911096G>T
CLNSRC
CLNACC