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rs374726386

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs374726386(A;A)
Make rs374726386(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position120738552
GeneACADS
is asnp
is mentioned by
dbSNPrs374726386
ebirs374726386
HLIrs374726386
Exacrs374726386
Varsomers374726386
Maprs374726386
PheGenIrs374726386
hapmaprs374726386
1000 genomesrs374726386
hgdprs374726386
ensemblrs374726386
gopubmedrs374726386
geneviewrs374726386
scholarrs374726386
googlers374726386
pharmgkbrs374726386
gwascentralrs374726386
openSNPrs374726386
23andMers374726386
23andMe allrs374726386
SNP Nexus

SNPshotrs374726386
SNPdbers374726386
MSV3drs374726386
GWAS Ctlgrs374726386
Max Magnitude0
ClinVar
Risk rs374726386(A;A)
Alt rs374726386(A;A)
Reference rs374726386(G;G)
Significance Pathogenic
Disease not specified
Variation info
Gene ACADS
CLNDBN not specified
Reversed 0
HGVS NC_000012.11:g.121176355G>A
CLNSRC
CLNACC RCV000185688.2,