rs151003641
From SNPedia
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 |
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, |