rs1057517842
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(ACTC;ACTC) | 0 | common in clinvar |
Make rs1057517842(ACTC;TTGTTTTAAGAGCGTTT) |
Make rs1057517842(TTGTTTTAAGAGCGTTT;TTGTTTTAAGAGCGTTT) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 9 |
Position | 132903750 |
Gene | TSC1 |
is a | snp |
is | mentioned by |
dbSNP | rs1057517842 |
dbSNP (classic) | rs1057517842 |
ClinGen | rs1057517842 |
ebi | rs1057517842 |
HLI | rs1057517842 |
Exac | rs1057517842 |
Gnomad | rs1057517842 |
Varsome | rs1057517842 |
LitVar | rs1057517842 |
Map | rs1057517842 |
PheGenI | rs1057517842 |
Biobank | rs1057517842 |
1000 genomes | rs1057517842 |
hgdp | rs1057517842 |
ensembl | rs1057517842 |
geneview | rs1057517842 |
scholar | rs1057517842 |
rs1057517842 | |
pharmgkb | rs1057517842 |
gwascentral | rs1057517842 |
openSNP | rs1057517842 |
23andMe | rs1057517842 |
SNPshot | rs1057517842 |
SNPdbe | rs1057517842 |
MSV3d | rs1057517842 |
GWAS Ctlg | rs1057517842 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057517842(TTGTTTTAAGAGCGTTT;TTGTTTTAAGAGCGTTT) |
Alt | rs1057517842(TTGTTTTAAGAGCGTTT;TTGTTTTAAGAGCGTTT) |
Reference | Rs1057517842(ACTC;ACTC) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | TSC1 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000009.11:g.135779137_135779140delGAGTinsAAACGCTCTTAAAACAA |
CLNSRC | |
CLNACC | RCV000412759.1, |