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rs140853839

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs140853839(C;T)
Make rs140853839(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position120738874
GeneACADS
is asnp
is mentioned by
dbSNPrs140853839
ebirs140853839
HLIrs140853839
Exacrs140853839
Varsomers140853839
Maprs140853839
PheGenIrs140853839
hapmaprs140853839
1000 genomesrs140853839
hgdprs140853839
ensemblrs140853839
gopubmedrs140853839
geneviewrs140853839
scholarrs140853839
googlers140853839
pharmgkbrs140853839
gwascentralrs140853839
openSNPrs140853839
23andMers140853839
23andMe allrs140853839
SNP Nexus

SNPshotrs140853839
SNPdbers140853839
MSV3drs140853839
GWAS Ctlgrs140853839
Max Magnitude0
ClinVar
Risk rs140853839(A;A) rs140853839(T;T)
Alt rs140853839(A;A) rs140853839(T;T)
Reference Rs140853839(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ACADS
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.121176677C>T
CLNSRC
CLNACC RCV000185690.2,