rs118203477
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(CT;CT) | 0 | common in clinvar |
Make rs118203477(-;-) |
Make rs118203477(-;CT) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 9 |
Position | 132911493 |
Gene | TSC1 |
is a | snp |
is | mentioned by |
dbSNP | rs118203477 |
dbSNP (classic) | rs118203477 |
ClinGen | rs118203477 |
ebi | rs118203477 |
HLI | rs118203477 |
Exac | rs118203477 |
Gnomad | rs118203477 |
Varsome | rs118203477 |
LitVar | rs118203477 |
Map | rs118203477 |
PheGenI | rs118203477 |
Biobank | rs118203477 |
1000 genomes | rs118203477 |
hgdp | rs118203477 |
ensembl | rs118203477 |
geneview | rs118203477 |
scholar | rs118203477 |
rs118203477 | |
pharmgkb | rs118203477 |
gwascentral | rs118203477 |
openSNP | rs118203477 |
23andMe | rs118203477 |
SNPshot | rs118203477 |
SNPdbe | rs118203477 |
MSV3d | rs118203477 |
GWAS Ctlg | rs118203477 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs118203477(-;-) |
Alt | rs118203477(-;-) |
Reference | Rs118203477(CT;CT) |
Significance | Pathogenic |
Disease | Tuberous sclerosis syndrome Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | TSC1 |
CLNDBN | Tuberous sclerosis syndrome Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000009.11:g.135786880_135786881delAG |
CLNSRC | Tuberous sclerosis database (TSC1) |
CLNACC | RCV000042387.2, RCV000491469.1, |