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rs368311455

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs368311455(C;T)
Make rs368311455(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position53211185
GeneCPT2
is asnp
is mentioned by
dbSNPrs368311455
ebirs368311455
HLIrs368311455
Exacrs368311455
Varsomers368311455
Maprs368311455
PheGenIrs368311455
hapmaprs368311455
1000 genomesrs368311455
hgdprs368311455
ensemblrs368311455
gopubmedrs368311455
geneviewrs368311455
scholarrs368311455
googlers368311455
pharmgkbrs368311455
gwascentralrs368311455
openSNPrs368311455
23andMers368311455
23andMe allrs368311455
SNP Nexus

SNPshotrs368311455
SNPdbers368311455
MSV3drs368311455
GWAS Ctlgrs368311455
Max Magnitude0
ClinVar
Risk rs368311455(T;T)
Alt rs368311455(T;T)
Reference rs368311455(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CPT2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.53676857C>T
CLNSRC
CLNACC RCV000185833.1,