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rs1057521114

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057521114(A;G)
Make rs1057521114(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position75732854
GeneACADM
is asnp
is mentioned by
dbSNPrs1057521114
dbSNP (old)rs1057521114
ClinGenrs1057521114
ebirs1057521114
HLIrs1057521114
Exacrs1057521114
Gnomadrs1057521114
Varsomers1057521114
Maprs1057521114
PheGenIrs1057521114
Biobankrs1057521114
1000 genomesrs1057521114
hgdprs1057521114
ensemblrs1057521114
gopubmedrs1057521114
geneviewrs1057521114
scholarrs1057521114
googlers1057521114
pharmgkbrs1057521114
gwascentralrs1057521114
openSNPrs1057521114
23andMers1057521114
23andMe allrs1057521114
SNPshotrs1057521114
SNPdbers1057521114
MSV3drs1057521114
GWAS Ctlgrs1057521114
Max Magnitude0
ClinVar
Risk rs1057521114(G;G)
Alt rs1057521114(G;G)
Reference Rs1057521114(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACADM
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.76198539A>G
CLNSRC
CLNACC RCV000439469.1,