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rs794727833

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794727833(A;A)
Make rs794727833(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position75739980
GeneACADM
is asnp
is mentioned by
dbSNPrs794727833
ebirs794727833
HLIrs794727833
Exacrs794727833
Varsomers794727833
Maprs794727833
PheGenIrs794727833
hapmaprs794727833
1000 genomesrs794727833
hgdprs794727833
ensemblrs794727833
gopubmedrs794727833
geneviewrs794727833
scholarrs794727833
googlers794727833
pharmgkbrs794727833
gwascentralrs794727833
openSNPrs794727833
23andMers794727833
23andMe allrs794727833
SNP Nexus

SNPshotrs794727833
SNPdbers794727833
MSV3drs794727833
GWAS Ctlgrs794727833
Max Magnitude0
ClinVar
Risk rs794727833(A;A)
Alt rs794727833(A;A)
Reference rs794727833(G;G)
Significance Unknown
Disease not provided
Variation info
Gene ACADM
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.76205665G>A
CLNSRC
CLNACC RCV000179695.1,