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rs754477154

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs754477154(A;A)
Make rs754477154(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position32984734
GeneAPTX
is asnp
is mentioned by
dbSNPrs754477154
ebirs754477154
HLIrs754477154
Exacrs754477154
Varsomers754477154
Maprs754477154
PheGenIrs754477154
hapmaprs754477154
1000 genomesrs754477154
hgdprs754477154
ensemblrs754477154
gopubmedrs754477154
geneviewrs754477154
scholarrs754477154
googlers754477154
pharmgkbrs754477154
gwascentralrs754477154
openSNPrs754477154
23andMers754477154
23andMe allrs754477154
SNP Nexus

SNPshotrs754477154
SNPdbers754477154
MSV3drs754477154
GWAS Ctlgrs754477154
Max Magnitude0
ClinVar
Risk rs754477154(A;A)
Alt rs754477154(A;A)
Reference rs754477154(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene APTX
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.32984732G>A
CLNSRC
CLNACC RCV000199604.1,