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rs183161718

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs183161718(C;T)
Make rs183161718(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position120739339
GeneACADS
is asnp
is mentioned by
dbSNPrs183161718
dbSNP (old)rs183161718
ClinGenrs183161718
ebirs183161718
HLIrs183161718
Exacrs183161718
Gnomadrs183161718
Varsomers183161718
LitVarrs183161718
Maprs183161718
PheGenIrs183161718
Biobankrs183161718
1000 genomesrs183161718
hgdprs183161718
ensemblrs183161718
gopubmedrs183161718
geneviewrs183161718
scholarrs183161718
googlers183161718
pharmgkbrs183161718
gwascentralrs183161718
openSNPrs183161718
23andMers183161718
23andMe allrs183161718
SNPshotrs183161718
SNPdbers183161718
MSV3drs183161718
GWAS Ctlgrs183161718
Max Magnitude0
ClinVar
Risk rs183161718(T;T)
Alt rs183161718(T;T)
Reference Rs183161718(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACADS
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.121177142C>T
CLNSRC
CLNACC RCV000489608.1,