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rs796051942

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796051942(A;A)
Make rs796051942(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position53210305
GeneCPT2
is asnp
is mentioned by
dbSNPrs796051942
ebirs796051942
HLIrs796051942
Exacrs796051942
Varsomers796051942
Maprs796051942
PheGenIrs796051942
hapmaprs796051942
1000 genomesrs796051942
hgdprs796051942
ensemblrs796051942
gopubmedrs796051942
geneviewrs796051942
scholarrs796051942
googlers796051942
pharmgkbrs796051942
gwascentralrs796051942
openSNPrs796051942
23andMers796051942
23andMe allrs796051942
SNP Nexus

SNPshotrs796051942
SNPdbers796051942
MSV3drs796051942
GWAS Ctlgrs796051942
Max Magnitude0
ClinVar
Risk rs796051942(A;A)
Alt rs796051942(A;A)
Reference rs796051942(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CPT2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.53675977C>A
CLNSRC
CLNACC RCV000185830.1,