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rs747593459

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs747593459(G;G)
Make rs747593459(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position75750527
GeneACADM
is asnp
is mentioned by
dbSNPrs747593459
ebirs747593459
HLIrs747593459
Exacrs747593459
Varsomers747593459
Maprs747593459
PheGenIrs747593459
hapmaprs747593459
1000 genomesrs747593459
hgdprs747593459
ensemblrs747593459
gopubmedrs747593459
geneviewrs747593459
scholarrs747593459
googlers747593459
pharmgkbrs747593459
gwascentralrs747593459
openSNPrs747593459
23andMers747593459
23andMe allrs747593459
SNP Nexus

SNPshotrs747593459
SNPdbers747593459
MSV3drs747593459
GWAS Ctlgrs747593459
Max Magnitude0
ClinVar
Risk rs747593459(G;G)
Alt rs747593459(G;G)
Reference rs747593459(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACADM
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.76216212T>G
CLNSRC
CLNACC RCV000185678.1,