rs756181906
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs756181906(G;T) |
Make rs756181906(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 16 |
Position | 2496828 |
Gene | TBC1D24 |
is a | snp |
is | mentioned by |
dbSNP | rs756181906 |
dbSNP (classic) | rs756181906 |
ClinGen | rs756181906 |
ebi | rs756181906 |
HLI | rs756181906 |
Exac | rs756181906 |
Gnomad | rs756181906 |
Varsome | rs756181906 |
LitVar | rs756181906 |
Map | rs756181906 |
PheGenI | rs756181906 |
Biobank | rs756181906 |
1000 genomes | rs756181906 |
hgdp | rs756181906 |
ensembl | rs756181906 |
geneview | rs756181906 |
scholar | rs756181906 |
rs756181906 | |
pharmgkb | rs756181906 |
gwascentral | rs756181906 |
openSNP | rs756181906 |
23andMe | rs756181906 |
SNPshot | rs756181906 |
SNPdbe | rs756181906 |
MSV3d | rs756181906 |
GWAS Ctlg | rs756181906 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs756181906(A;A) rs756181906(T;T) |
Alt | rs756181906(A;A) rs756181906(T;T) |
Reference | Rs756181906(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | TBC1D24 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000016.9:g.2546829G>T |
CLNSRC | |
CLNACC | RCV000189690.2, |