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rs1057518408

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518408(A;G)
Make rs1057518408(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position75749449
GeneACADM
is asnp
is mentioned by
dbSNPrs1057518408
dbSNP (old)rs1057518408
ClinGenrs1057518408
ebirs1057518408
HLIrs1057518408
Exacrs1057518408
Gnomadrs1057518408
Varsomers1057518408
Maprs1057518408
PheGenIrs1057518408
Biobankrs1057518408
1000 genomesrs1057518408
hgdprs1057518408
ensemblrs1057518408
gopubmedrs1057518408
geneviewrs1057518408
scholarrs1057518408
googlers1057518408
pharmgkbrs1057518408
gwascentralrs1057518408
openSNPrs1057518408
23andMers1057518408
23andMe allrs1057518408
SNPshotrs1057518408
SNPdbers1057518408
MSV3drs1057518408
GWAS Ctlgrs1057518408
Max Magnitude0
ClinVar
Risk rs1057518408(G;G)
Alt rs1057518408(G;G)
Reference Rs1057518408(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACADM
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.76215134A>G
CLNSRC
CLNACC RCV000412735.1,