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

rs796051899

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796051899(A;A)
Make rs796051899(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position75733558
GeneACADM
is asnp
is mentioned by
dbSNPrs796051899
ebirs796051899
HLIrs796051899
Exacrs796051899
Varsomers796051899
Maprs796051899
PheGenIrs796051899
hapmaprs796051899
1000 genomesrs796051899
hgdprs796051899
ensemblrs796051899
gopubmedrs796051899
geneviewrs796051899
scholarrs796051899
googlers796051899
pharmgkbrs796051899
gwascentralrs796051899
openSNPrs796051899
23andMers796051899
23andMe allrs796051899
SNP Nexus

SNPshotrs796051899
SNPdbers796051899
MSV3drs796051899
GWAS Ctlgrs796051899
Max Magnitude0
ClinVar
Risk rs796051899(A;A)
Alt rs796051899(A;A)
Reference rs796051899(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACADM
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.76199243G>A
CLNSRC
CLNACC RCV000185672.1,