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rs796051944

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796051944(C;T)
Make rs796051944(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position53210393
GeneCPT2
is asnp
is mentioned by
dbSNPrs796051944
ebirs796051944
HLIrs796051944
Exacrs796051944
Varsomers796051944
Maprs796051944
PheGenIrs796051944
hapmaprs796051944
1000 genomesrs796051944
hgdprs796051944
ensemblrs796051944
gopubmedrs796051944
geneviewrs796051944
scholarrs796051944
googlers796051944
pharmgkbrs796051944
gwascentralrs796051944
openSNPrs796051944
23andMers796051944
23andMe allrs796051944
SNP Nexus

SNPshotrs796051944
SNPdbers796051944
MSV3drs796051944
GWAS Ctlgrs796051944
Max Magnitude0
ClinVar
Risk rs796051944(T;T)
Alt rs796051944(T;T)
Reference rs796051944(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CPT2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.53676065C>T
CLNSRC
CLNACC RCV000185839.1,