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rs144076460

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs144076460(A;A)
Make rs144076460(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position32989874
GeneAPTX
is asnp
is mentioned by
dbSNPrs144076460
ebirs144076460
HLIrs144076460
Exacrs144076460
Varsomers144076460
Maprs144076460
PheGenIrs144076460
hapmaprs144076460
1000 genomesrs144076460
hgdprs144076460
ensemblrs144076460
gopubmedrs144076460
geneviewrs144076460
scholarrs144076460
googlers144076460
pharmgkbrs144076460
gwascentralrs144076460
openSNPrs144076460
23andMers144076460
23andMe allrs144076460
SNP Nexus

SNPshotrs144076460
SNPdbers144076460
MSV3drs144076460
GWAS Ctlgrs144076460
Max Magnitude0
ClinVar
Risk rs144076460(A;A)
Alt rs144076460(A;A)
Reference rs144076460(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APTX
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.32989872C>A
CLNSRC
CLNACC RCV000200146.2,