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rs863223896

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223896(A;A)
Make rs863223896(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position141621769
GeneAGK
is asnp
is mentioned by
dbSNPrs863223896
ebirs863223896
HLIrs863223896
Exacrs863223896
Varsomers863223896
Maprs863223896
PheGenIrs863223896
hapmaprs863223896
1000 genomesrs863223896
hgdprs863223896
ensemblrs863223896
gopubmedrs863223896
geneviewrs863223896
scholarrs863223896
googlers863223896
pharmgkbrs863223896
gwascentralrs863223896
openSNPrs863223896
23andMers863223896
23andMe allrs863223896
SNP Nexus

SNPshotrs863223896
SNPdbers863223896
MSV3drs863223896
GWAS Ctlgrs863223896
Max Magnitude0
ClinVar
Risk rs863223896(A;A)
Alt rs863223896(A;A)
Reference rs863223896(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AGK
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.141321569G>A
CLNSRC
CLNACC RCV000198825.1,