Have questions? Visit https://www.reddit.com/r/SNPedia

rs537072819

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs537072819(C;T)
Make rs537072819(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position120739365
GeneACADS
is asnp
is mentioned by
dbSNPrs537072819
ebirs537072819
HLIrs537072819
Exacrs537072819
Varsomers537072819
Maprs537072819
PheGenIrs537072819
hapmaprs537072819
1000 genomesrs537072819
hgdprs537072819
ensemblrs537072819
gopubmedrs537072819
geneviewrs537072819
scholarrs537072819
googlers537072819
pharmgkbrs537072819
gwascentralrs537072819
openSNPrs537072819
23andMers537072819
23andMe allrs537072819
SNP Nexus

SNPshotrs537072819
SNPdbers537072819
MSV3drs537072819
GWAS Ctlgrs537072819
Max Magnitude0
ClinVar
Risk rs537072819(T;T)
Alt rs537072819(T;T)
Reference rs537072819(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene ACADS
CLNDBN not specified
Reversed 0
HGVS NC_000012.11:g.121177168C>T
CLNSRC
CLNACC RCV000185703.2,