Have questions? Visit https://www.reddit.com/r/SNPedia

rs515726178

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs515726178(-;-)
Make rs515726178(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position53213355
GeneCPT2
is asnp
is mentioned by
dbSNPrs515726178
ebirs515726178
HLIrs515726178
Exacrs515726178
Varsomers515726178
Maprs515726178
PheGenIrs515726178
hapmaprs515726178
1000 genomesrs515726178
hgdprs515726178
ensemblrs515726178
gopubmedrs515726178
geneviewrs515726178
scholarrs515726178
googlers515726178
pharmgkbrs515726178
gwascentralrs515726178
openSNPrs515726178
23andMers515726178
23andMe allrs515726178
SNP Nexus

SNPshotrs515726178
SNPdbers515726178
MSV3drs515726178
GWAS Ctlgrs515726178
Max Magnitude0
ClinVar
Risk rs515726178(;)
Alt rs515726178(;)
Reference rs515726178(C;C)
Significance Pathogenic
Disease Carnitine palmitoyltransferase II deficiency
Variation info
Gene CPT2
CLNDBN Carnitine palmitoyltransferase II deficiency
Reversed 0
HGVS NC_000001.10:g.53679027delC
CLNSRC
CLNACC RCV000202525.1,