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rs878853106

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853106(A;A)
Make rs878853106(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position75749560
GeneACADM
is asnp
is mentioned by
dbSNPrs878853106
ebirs878853106
HLIrs878853106
Exacrs878853106
Varsomers878853106
Maprs878853106
PheGenIrs878853106
hapmaprs878853106
1000 genomesrs878853106
hgdprs878853106
ensemblrs878853106
gopubmedrs878853106
geneviewrs878853106
scholarrs878853106
googlers878853106
pharmgkbrs878853106
gwascentralrs878853106
openSNPrs878853106
23andMers878853106
23andMe allrs878853106
SNP Nexus

SNPshotrs878853106
SNPdbers878853106
MSV3drs878853106
GWAS Ctlgrs878853106
Max Magnitude0
ClinVar
Risk rs878853106(A;A)
Alt rs878853106(A;A)
Reference rs878853106(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ACADM
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.76215245G>A
CLNSRC
CLNACC RCV000224576.1,