rs119473032
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs119473032(A;G) |
Make rs119473032(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 20253576 |
Gene | LZTS1 |
is a | snp |
is | mentioned by |
dbSNP | rs119473032 |
dbSNP (classic) | rs119473032 |
ClinGen | rs119473032 |
ebi | rs119473032 |
HLI | rs119473032 |
Exac | rs119473032 |
Gnomad | rs119473032 |
Varsome | rs119473032 |
LitVar | rs119473032 |
Map | rs119473032 |
PheGenI | rs119473032 |
Biobank | rs119473032 |
1000 genomes | rs119473032 |
hgdp | rs119473032 |
ensembl | rs119473032 |
geneview | rs119473032 |
scholar | rs119473032 |
rs119473032 | |
pharmgkb | rs119473032 |
gwascentral | rs119473032 |
openSNP | rs119473032 |
23andMe | rs119473032 |
SNPshot | rs119473032 |
SNPdbe | rs119473032 |
MSV3d | rs119473032 |
GWAS Ctlg | rs119473032 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs119473032(G;G) |
Alt | rs119473032(G;G) |
Reference | Rs119473032(A;A) |
Significance | Pathogenic |
Disease | Esophageal squamous cell carcinoma |
Variation | info |
Gene | LZTS1 |
CLNDBN | Esophageal squamous cell carcinoma, somatic |
Reversed | 1 |
HGVS | NC_000008.10:g.20111087T>C |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000004468.4, |