rs368311455

Orientation

plus

Stabilized

plus

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

Make rs368311455(C;T)

Make rs368311455(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

53211185

Gene

CPT2

is a	snp
is	mentioned by
dbSNP	rs368311455
dbSNP (classic)	rs368311455
ClinGen	rs368311455
ebi	rs368311455
HLI	rs368311455
Exac	rs368311455
Gnomad	rs368311455
Varsome	rs368311455
LitVar	rs368311455
Map	rs368311455
PheGenI	rs368311455
Biobank	rs368311455
1000 genomes	rs368311455
hgdp	rs368311455
ensembl	rs368311455
geneview	rs368311455
scholar	rs368311455
google	rs368311455
pharmgkb	rs368311455
gwascentral	rs368311455
openSNP	rs368311455
23andMe	rs368311455
SNPshot	rs368311455
SNPdbe	rs368311455
MSV3d	rs368311455
GWAS Ctlg	rs368311455

Max Magnitude

0

ClinVar
Risk	rs368311455(T;T)
Alt	rs368311455(T;T)
Reference	Rs368311455(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CPT2
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.53676857C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000185833.1,