rs730880015
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs730880015(-;-) |
Make rs730880015(-;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 15 |
Position | 57243507 |
Gene | TCF12 |
is a | snp |
is | mentioned by |
dbSNP | rs730880015 |
dbSNP (classic) | rs730880015 |
ClinGen | rs730880015 |
ebi | rs730880015 |
HLI | rs730880015 |
Exac | rs730880015 |
Gnomad | rs730880015 |
Varsome | rs730880015 |
LitVar | rs730880015 |
Map | rs730880015 |
PheGenI | rs730880015 |
Biobank | rs730880015 |
1000 genomes | rs730880015 |
hgdp | rs730880015 |
ensembl | rs730880015 |
geneview | rs730880015 |
scholar | rs730880015 |
rs730880015 | |
pharmgkb | rs730880015 |
gwascentral | rs730880015 |
openSNP | rs730880015 |
23andMe | rs730880015 |
SNPshot | rs730880015 |
SNPdbe | rs730880015 |
MSV3d | rs730880015 |
GWAS Ctlg | rs730880015 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs730880015(-;-) |
Alt | rs730880015(-;-) |
Reference | Rs730880015(G;G) |
Significance | Pathogenic |
Disease | Craniosynostosis 3 |
Variation | info |
Gene | TCF12 |
CLNDBN | Craniosynostosis 3 |
Reversed | 0 |
HGVS | NC_000015.9:g.57535705delG |
CLNSRC | |
CLNACC | RCV000157615.1, |