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rs373638740

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs373638740(C;T)
Make rs373638740(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position53210365
GeneCPT2
is asnp
is mentioned by
dbSNPrs373638740
ebirs373638740
HLIrs373638740
Exacrs373638740
Varsomers373638740
Maprs373638740
PheGenIrs373638740
hapmaprs373638740
1000 genomesrs373638740
hgdprs373638740
ensemblrs373638740
gopubmedrs373638740
geneviewrs373638740
scholarrs373638740
googlers373638740
pharmgkbrs373638740
gwascentralrs373638740
openSNPrs373638740
23andMers373638740
23andMe allrs373638740
SNP Nexus

SNPshotrs373638740
SNPdbers373638740
MSV3drs373638740
GWAS Ctlgrs373638740
Max Magnitude0
ClinVar
Risk rs373638740(T;T)
Alt rs373638740(T;T)
Reference rs373638740(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CPT2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.53676037C>T
CLNSRC
CLNACC RCV000185831.1,