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rs796051901

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs796051901(-;-)
Make rs796051901(-;AG)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position75750483
GeneACADM
is asnp
is mentioned by
dbSNPrs796051901
ebirs796051901
HLIrs796051901
Exacrs796051901
Varsomers796051901
Maprs796051901
PheGenIrs796051901
hapmaprs796051901
1000 genomesrs796051901
hgdprs796051901
ensemblrs796051901
gopubmedrs796051901
geneviewrs796051901
scholarrs796051901
googlers796051901
pharmgkbrs796051901
gwascentralrs796051901
openSNPrs796051901
23andMers796051901
23andMe allrs796051901
SNP Nexus

SNPshotrs796051901
SNPdbers796051901
MSV3drs796051901
GWAS Ctlgrs796051901
Max Magnitude0
ClinVar
Risk rs796051901(;)
Alt rs796051901(;)
Reference rs796051901(AG;AG)
Significance Pathogenic
Disease not provided
Variation info
Gene ACADM
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.76216168_76216169delAG
CLNSRC
CLNACC RCV000185676.1,