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rs863223887

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223887(A;C)
Make rs863223887(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position226984230
GeneADCK3
is asnp
is mentioned by
dbSNPrs863223887
ebirs863223887
HLIrs863223887
Exacrs863223887
Varsomers863223887
Maprs863223887
PheGenIrs863223887
hapmaprs863223887
1000 genomesrs863223887
hgdprs863223887
ensemblrs863223887
gopubmedrs863223887
geneviewrs863223887
scholarrs863223887
googlers863223887
pharmgkbrs863223887
gwascentralrs863223887
openSNPrs863223887
23andMers863223887
23andMe allrs863223887
SNP Nexus

SNPshotrs863223887
SNPdbers863223887
MSV3drs863223887
GWAS Ctlgrs863223887
Max Magnitude0
ClinVar
Risk rs863223887(C;C)
Alt rs863223887(C;C)
Reference rs863223887(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ADCK3
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.227171931A>C
CLNSRC
CLNACC RCV000196096.1,