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rs1057517729

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517729(-;-)
Make rs1057517729(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position53210526
GeneCPT2
is asnp
is mentioned by
dbSNPrs1057517729
dbSNP (old)rs1057517729
ClinGenrs1057517729
ebirs1057517729
HLIrs1057517729
Exacrs1057517729
Gnomadrs1057517729
Varsomers1057517729
Maprs1057517729
PheGenIrs1057517729
Biobankrs1057517729
1000 genomesrs1057517729
hgdprs1057517729
ensemblrs1057517729
gopubmedrs1057517729
geneviewrs1057517729
scholarrs1057517729
googlers1057517729
pharmgkbrs1057517729
gwascentralrs1057517729
openSNPrs1057517729
23andMers1057517729
23andMe allrs1057517729
SNPshotrs1057517729
SNPdbers1057517729
MSV3drs1057517729
GWAS Ctlgrs1057517729
Max Magnitude0
ClinVar
Risk rs1057517729(-;-)
Alt rs1057517729(-;-)
Reference Rs1057517729(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CPT2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.53676198delC
CLNSRC
CLNACC RCV000413363.1,