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rs796051898

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796051898(C;C)
Make rs796051898(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position75733530
GeneACADM
is asnp
is mentioned by
dbSNPrs796051898
ebirs796051898
HLIrs796051898
Exacrs796051898
Varsomers796051898
Maprs796051898
PheGenIrs796051898
hapmaprs796051898
1000 genomesrs796051898
hgdprs796051898
ensemblrs796051898
gopubmedrs796051898
geneviewrs796051898
scholarrs796051898
googlers796051898
pharmgkbrs796051898
gwascentralrs796051898
openSNPrs796051898
23andMers796051898
23andMe allrs796051898
SNP Nexus

SNPshotrs796051898
SNPdbers796051898
MSV3drs796051898
GWAS Ctlgrs796051898
Max Magnitude0
ClinVar
Risk rs796051898(C;C)
Alt rs796051898(C;C)
Reference rs796051898(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACADM
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.76199215G>C
CLNSRC
CLNACC RCV000185671.1,