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rs1057520214

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057520214(A;C)
Make rs1057520214(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position75732702
GeneACADM
is asnp
is mentioned by
dbSNPrs1057520214
dbSNP (classic)rs1057520214
ClinGenrs1057520214
ebirs1057520214
HLIrs1057520214
Exacrs1057520214
Gnomadrs1057520214
Varsomers1057520214
LitVarrs1057520214
Maprs1057520214
PheGenIrs1057520214
Biobankrs1057520214
1000 genomesrs1057520214
hgdprs1057520214
ensemblrs1057520214
geneviewrs1057520214
scholarrs1057520214
googlers1057520214
pharmgkbrs1057520214
gwascentralrs1057520214
openSNPrs1057520214
23andMers1057520214
23andMe allrs1057520214
SNPshotrs1057520214
SNPdbers1057520214
MSV3drs1057520214
GWAS Ctlgrs1057520214
Max Magnitude0
ClinVar
Risk rs1057520214(C;C)
Alt rs1057520214(C;C)
Reference Rs1057520214(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACADM
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.76198387A>C
CLNSRC
CLNACC RCV000422626.1,