rs759454598
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs759454598(G;T) |
Make rs759454598(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 13 |
Position | 40799092 |
Gene | SLC25A15, TPTE2P5 |
is a | snp |
is | mentioned by |
dbSNP | rs759454598 |
dbSNP (classic) | rs759454598 |
ClinGen | rs759454598 |
ebi | rs759454598 |
HLI | rs759454598 |
Exac | rs759454598 |
Gnomad | rs759454598 |
Varsome | rs759454598 |
LitVar | rs759454598 |
Map | rs759454598 |
PheGenI | rs759454598 |
Biobank | rs759454598 |
1000 genomes | rs759454598 |
hgdp | rs759454598 |
ensembl | rs759454598 |
geneview | rs759454598 |
scholar | rs759454598 |
rs759454598 | |
pharmgkb | rs759454598 |
gwascentral | rs759454598 |
openSNP | rs759454598 |
23andMe | rs759454598 |
SNPshot | rs759454598 |
SNPdbe | rs759454598 |
MSV3d | rs759454598 |
GWAS Ctlg | rs759454598 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs759454598(A;A) rs759454598(C;C) rs759454598(T;T) |
Alt | rs759454598(A;A) rs759454598(C;C) rs759454598(T;T) |
Reference | Rs759454598(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SLC25A15 TPTE2P5 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000013.10:g.41373228G>C |
CLNSRC | |
CLNACC | RCV000484190.1, |