rs151003641

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs151003641(C;T)

Make rs151003641(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

53210722

Gene

CPT2

is a	snp
is	mentioned by
dbSNP	rs151003641
dbSNP (classic)	rs151003641
ClinGen	rs151003641
ebi	rs151003641
HLI	rs151003641
Exac	rs151003641
Gnomad	rs151003641
Varsome	rs151003641
LitVar	rs151003641
Map	rs151003641
PheGenI	rs151003641
Biobank	rs151003641
1000 genomes	rs151003641
hgdp	rs151003641
ensembl	rs151003641
geneview	rs151003641
scholar	rs151003641
google	rs151003641
pharmgkb	rs151003641
gwascentral	rs151003641
openSNP	rs151003641
23andMe	rs151003641
SNPshot	rs151003641
SNPdbe	rs151003641
MSV3d	rs151003641
GWAS Ctlg	rs151003641

Max Magnitude

0

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	RCV000185832.2,