rs1057517668
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs1057517668(C;T) |
Make rs1057517668(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 3 |
Position | 147413372 |
Gene | ZIC1 |
is a | snp |
is | mentioned by |
dbSNP | rs1057517668 |
dbSNP (classic) | rs1057517668 |
ClinGen | rs1057517668 |
ebi | rs1057517668 |
HLI | rs1057517668 |
Exac | rs1057517668 |
Gnomad | rs1057517668 |
Varsome | rs1057517668 |
LitVar | rs1057517668 |
Map | rs1057517668 |
PheGenI | rs1057517668 |
Biobank | rs1057517668 |
1000 genomes | rs1057517668 |
hgdp | rs1057517668 |
ensembl | rs1057517668 |
geneview | rs1057517668 |
scholar | rs1057517668 |
rs1057517668 | |
pharmgkb | rs1057517668 |
gwascentral | rs1057517668 |
openSNP | rs1057517668 |
23andMe | rs1057517668 |
SNPshot | rs1057517668 |
SNPdbe | rs1057517668 |
MSV3d | rs1057517668 |
GWAS Ctlg | rs1057517668 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057517668(T;T) |
Alt | rs1057517668(T;T) |
Reference | Rs1057517668(C;C) |
Significance | Pathogenic |
Disease | Craniosynostosis 6 |
Variation | info |
Gene | ZIC1 |
CLNDBN | Craniosynostosis 6 |
Reversed | 0 |
HGVS | NC_000003.11:g.147131159C>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000412596.1, |