rs1064795637
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(GAGT;GAGT) | 0 | common in clinvar |
Chromosome | 9 |
Position | 95480384 |
Gene | PTCH1 |
is a | snp |
is | mentioned by |
dbSNP | rs1064795637 |
dbSNP (classic) | rs1064795637 |
ClinGen | rs1064795637 |
ebi | rs1064795637 |
HLI | rs1064795637 |
Exac | rs1064795637 |
Gnomad | rs1064795637 |
Varsome | rs1064795637 |
LitVar | rs1064795637 |
Map | rs1064795637 |
PheGenI | rs1064795637 |
Biobank | rs1064795637 |
1000 genomes | rs1064795637 |
hgdp | rs1064795637 |
ensembl | rs1064795637 |
geneview | rs1064795637 |
scholar | rs1064795637 |
rs1064795637 | |
pharmgkb | rs1064795637 |
gwascentral | rs1064795637 |
openSNP | rs1064795637 |
23andMe | rs1064795637 |
SNPshot | rs1064795637 |
SNPdbe | rs1064795637 |
MSV3d | rs1064795637 |
GWAS Ctlg | rs1064795637 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1064795637(-;-) |
Alt | rs1064795637(-;-) |
Reference | Rs1064795637(GAGT;GAGT) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | PTCH1 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000009.11:g.98242666_98242669delACTC |
CLNSRC | |
CLNACC | RCV000479558.1, |