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rs151003641

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151003641(C;T)
Make rs151003641(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position53210722
GeneCPT2
is asnp
is mentioned by
dbSNPrs151003641
ebirs151003641
HLIrs151003641
Exacrs151003641
Varsomers151003641
Maprs151003641
PheGenIrs151003641
hapmaprs151003641
1000 genomesrs151003641
hgdprs151003641
ensemblrs151003641
gopubmedrs151003641
geneviewrs151003641
scholarrs151003641
googlers151003641
pharmgkbrs151003641
gwascentralrs151003641
openSNPrs151003641
23andMers151003641
23andMe allrs151003641
SNP Nexus

SNPshotrs151003641
SNPdbers151003641
MSV3drs151003641
GWAS Ctlgrs151003641
Max Magnitude0
ClinVar
Risk rs151003641(T;T)
Alt rs151003641(T;T)
Reference rs151003641(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CPT2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.53676394C>T
CLNSRC
CLNACC RCV000185832.1,