rs118203402
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;G) | 6.3 | Tuberous Sclerosis Complex |
(G;G) | 0 | common in clinvar |
Make rs118203402(C;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 9 |
Position | 132921913 |
Gene | TSC1 |
is a | snp |
is | mentioned by |
dbSNP | rs118203402 |
dbSNP (classic) | rs118203402 |
ClinGen | rs118203402 |
ebi | rs118203402 |
HLI | rs118203402 |
Exac | rs118203402 |
Gnomad | rs118203402 |
Varsome | rs118203402 |
LitVar | rs118203402 |
Map | rs118203402 |
PheGenI | rs118203402 |
Biobank | rs118203402 |
1000 genomes | rs118203402 |
hgdp | rs118203402 |
ensembl | rs118203402 |
geneview | rs118203402 |
scholar | rs118203402 |
rs118203402 | |
pharmgkb | rs118203402 |
gwascentral | rs118203402 |
openSNP | rs118203402 |
23andMe | rs118203402 |
SNPshot | rs118203402 |
SNPdbe | rs118203402 |
MSV3d | rs118203402 |
GWAS Ctlg | rs118203402 |
Max Magnitude | 6.3 |
ClinVar | |
---|---|
Risk | rs118203402(A;A) rs118203402(C;C) |
Alt | rs118203402(A;A) rs118203402(C;C) |
Reference | Rs118203402(G;G) |
Significance | Probable-Pathogenic |
Disease | Tuberous sclerosis syndrome not provided |
Variation | info |
Gene | TSC1 |
CLNDBN | Tuberous sclerosis syndrome not provided |
Reversed | 1 |
HGVS | NC_000009.11:g.135797300C>G |
CLNSRC | Tuberous sclerosis database (TSC1) |
CLNACC | RCV000042311.2, RCV000442086.1, |