rs761944958

Orientation

plus

Stabilized

plus

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

Make rs761944958(C;T)

Make rs761944958(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

68780704

Gene

CPT1A

is a	snp
is	mentioned by
dbSNP	rs761944958
dbSNP (classic)	rs761944958
ClinGen	rs761944958
ebi	rs761944958
HLI	rs761944958
Exac	rs761944958
Gnomad	rs761944958
Varsome	rs761944958
LitVar	rs761944958
Map	rs761944958
PheGenI	rs761944958
Biobank	rs761944958
1000 genomes	rs761944958
hgdp	rs761944958
ensembl	rs761944958
geneview	rs761944958
scholar	rs761944958
google	rs761944958
pharmgkb	rs761944958
gwascentral	rs761944958
openSNP	rs761944958
23andMe	rs761944958
SNPshot	rs761944958
SNPdbe	rs761944958
MSV3d	rs761944958
GWAS Ctlg	rs761944958

Max Magnitude

0

ClinVar
Risk	rs761944958(A;A) rs761944958(T;T)
Alt	rs761944958(A;A) rs761944958(T;T)
Reference	Rs761944958(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CPT1A
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.68548172C>T
CLNSRC
CLNACC	RCV000413906.1,