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rs145466253

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs145466253(A;A)
Make rs145466253(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position120739314
GeneACADS
is asnp
is mentioned by
dbSNPrs145466253
ebirs145466253
HLIrs145466253
Exacrs145466253
Varsomers145466253
Maprs145466253
PheGenIrs145466253
hapmaprs145466253
1000 genomesrs145466253
hgdprs145466253
ensemblrs145466253
gopubmedrs145466253
geneviewrs145466253
scholarrs145466253
googlers145466253
pharmgkbrs145466253
gwascentralrs145466253
openSNPrs145466253
23andMers145466253
23andMe allrs145466253
SNP Nexus

SNPshotrs145466253
SNPdbers145466253
MSV3drs145466253
GWAS Ctlgrs145466253
Max Magnitude0
ClinVar
Risk rs145466253(A;A)
Alt rs145466253(A;A)
Reference rs145466253(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACADS
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.121177117G>A
CLNSRC
CLNACC RCV000185695.1,