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

rs761944958

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs761944958(C;T)
Make rs761944958(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position68780704
GeneCPT1A
is asnp
is mentioned by
dbSNPrs761944958
dbSNP (classic)rs761944958
ClinGenrs761944958
ebirs761944958
HLIrs761944958
Exacrs761944958
Gnomadrs761944958
Varsomers761944958
LitVarrs761944958
Maprs761944958
PheGenIrs761944958
Biobankrs761944958
1000 genomesrs761944958
hgdprs761944958
ensemblrs761944958
geneviewrs761944958
scholarrs761944958
googlers761944958
pharmgkbrs761944958
gwascentralrs761944958
openSNPrs761944958
23andMers761944958
23andMe allrs761944958
SNPshotrs761944958
SNPdbers761944958
MSV3drs761944958
GWAS Ctlgrs761944958
Max Magnitude0
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,