rs1057520063
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs1057520063(-;T) |
Make rs1057520063(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 7 |
Position | 41964641 |
Gene | GLI3 |
is a | snp |
is | mentioned by |
dbSNP | rs1057520063 |
dbSNP (classic) | rs1057520063 |
ClinGen | rs1057520063 |
ebi | rs1057520063 |
HLI | rs1057520063 |
Exac | rs1057520063 |
Gnomad | rs1057520063 |
Varsome | rs1057520063 |
LitVar | rs1057520063 |
Map | rs1057520063 |
PheGenI | rs1057520063 |
Biobank | rs1057520063 |
1000 genomes | rs1057520063 |
hgdp | rs1057520063 |
ensembl | rs1057520063 |
geneview | rs1057520063 |
scholar | rs1057520063 |
rs1057520063 | |
pharmgkb | rs1057520063 |
gwascentral | rs1057520063 |
openSNP | rs1057520063 |
23andMe | rs1057520063 |
SNPshot | rs1057520063 |
SNPdbe | rs1057520063 |
MSV3d | rs1057520063 |
GWAS Ctlg | rs1057520063 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057520063(T;T) |
Alt | rs1057520063(T;T) |
Reference | Rs1057520063(-;-) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | GLI3 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000007.13:g.42004240dupA |
CLNSRC | |
CLNACC | RCV000432432.1, |