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rs146453758

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs146453758(C;T)
Make rs146453758(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position128896520
GeneACAD9
is asnp
is mentioned by
dbSNPrs146453758
ebirs146453758
HLIrs146453758
Exacrs146453758
Varsomers146453758
Maprs146453758
PheGenIrs146453758
hapmaprs146453758
1000 genomesrs146453758
hgdprs146453758
ensemblrs146453758
gopubmedrs146453758
geneviewrs146453758
scholarrs146453758
googlers146453758
pharmgkbrs146453758
gwascentralrs146453758
openSNPrs146453758
23andMers146453758
23andMe allrs146453758
SNP Nexus

SNPshotrs146453758
SNPdbers146453758
MSV3drs146453758
GWAS Ctlgrs146453758
Max Magnitude0
ClinVar
Risk rs146453758(T;T)
Alt rs146453758(T;T)
Reference rs146453758(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACAD9
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.128615363C>T
CLNSRC
CLNACC RCV000200617.1,