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rs863223895

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223895(A;A)
Make rs863223895(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position141555469
GeneAGK
is asnp
is mentioned by
dbSNPrs863223895
ebirs863223895
HLIrs863223895
Exacrs863223895
Varsomers863223895
Maprs863223895
PheGenIrs863223895
hapmaprs863223895
1000 genomesrs863223895
hgdprs863223895
ensemblrs863223895
gopubmedrs863223895
geneviewrs863223895
scholarrs863223895
googlers863223895
pharmgkbrs863223895
gwascentralrs863223895
openSNPrs863223895
23andMers863223895
23andMe allrs863223895
SNP Nexus

SNPshotrs863223895
SNPdbers863223895
MSV3drs863223895
GWAS Ctlgrs863223895
Max Magnitude0
ClinVar
Risk rs863223895(A,C;A,C)
Alt rs863223895(A,C;A,C)
Reference rs863223895(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene AGK
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.141255269G>A; NC_000007.13:g.141255269G>C
CLNSRC
CLNACC RCV000198714.1, RCV000200556.2,