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rs747339462

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs747339462(C;T)
Make rs747339462(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position120737107
GeneACADS
is asnp
is mentioned by
dbSNPrs747339462
ebirs747339462
HLIrs747339462
Exacrs747339462
Varsomers747339462
Maprs747339462
PheGenIrs747339462
hapmaprs747339462
1000 genomesrs747339462
hgdprs747339462
ensemblrs747339462
gopubmedrs747339462
geneviewrs747339462
scholarrs747339462
googlers747339462
pharmgkbrs747339462
gwascentralrs747339462
openSNPrs747339462
23andMers747339462
23andMe allrs747339462
SNP Nexus

SNPshotrs747339462
SNPdbers747339462
MSV3drs747339462
GWAS Ctlgrs747339462
Max Magnitude0
ClinVar
Risk rs747339462(T;T)
Alt rs747339462(T;T)
Reference rs747339462(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACADS
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.121174910C>T
CLNSRC
CLNACC RCV000185681.1,