rs1064796659
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(CAGG;CAGG) | 0 | common in clinvar |
Chromosome | X |
Position | 154414155 |
Gene | TAZ |
is a | snp |
is | mentioned by |
dbSNP | rs1064796659 |
dbSNP (classic) | rs1064796659 |
ClinGen | rs1064796659 |
ebi | rs1064796659 |
HLI | rs1064796659 |
Exac | rs1064796659 |
Gnomad | rs1064796659 |
Varsome | rs1064796659 |
LitVar | rs1064796659 |
Map | rs1064796659 |
PheGenI | rs1064796659 |
Biobank | rs1064796659 |
1000 genomes | rs1064796659 |
hgdp | rs1064796659 |
ensembl | rs1064796659 |
geneview | rs1064796659 |
scholar | rs1064796659 |
rs1064796659 | |
pharmgkb | rs1064796659 |
gwascentral | rs1064796659 |
openSNP | rs1064796659 |
23andMe | rs1064796659 |
SNPshot | rs1064796659 |
SNPdbe | rs1064796659 |
MSV3d | rs1064796659 |
GWAS Ctlg | rs1064796659 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1064796659(-;-) |
Alt | rs1064796659(-;-) |
Reference | Rs1064796659(CAGG;CAGG) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | TAZ |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000023.10:g.153642492_153642495delGGCA |
CLNSRC | |
CLNACC | RCV000482188.1, |