rs748302886
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs748302886(C;T) |
Make rs748302886(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 16 |
Position | 2496827 |
Gene | TBC1D24 |
is a | snp |
is | mentioned by |
dbSNP | rs748302886 |
dbSNP (classic) | rs748302886 |
ClinGen | rs748302886 |
ebi | rs748302886 |
HLI | rs748302886 |
Exac | rs748302886 |
Gnomad | rs748302886 |
Varsome | rs748302886 |
LitVar | rs748302886 |
Map | rs748302886 |
PheGenI | rs748302886 |
Biobank | rs748302886 |
1000 genomes | rs748302886 |
hgdp | rs748302886 |
ensembl | rs748302886 |
geneview | rs748302886 |
scholar | rs748302886 |
rs748302886 | |
pharmgkb | rs748302886 |
gwascentral | rs748302886 |
openSNP | rs748302886 |
23andMe | rs748302886 |
SNPshot | rs748302886 |
SNPdbe | rs748302886 |
MSV3d | rs748302886 |
GWAS Ctlg | rs748302886 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs748302886(T;T) |
Alt | rs748302886(T;T) |
Reference | Rs748302886(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | TBC1D24 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000016.9:g.2546828C>T |
CLNSRC | |
CLNACC | RCV000492824.1, |