rs398122376
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs398122376(-;AAAA) |
Make rs398122376(AAAA;AAAA) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 170719753 |
Gene | PRRX1 |
is a | snp |
is | mentioned by |
dbSNP | rs398122376 |
dbSNP (classic) | rs398122376 |
ClinGen | rs398122376 |
ebi | rs398122376 |
HLI | rs398122376 |
Exac | rs398122376 |
Gnomad | rs398122376 |
Varsome | rs398122376 |
LitVar | rs398122376 |
Map | rs398122376 |
PheGenI | rs398122376 |
Biobank | rs398122376 |
1000 genomes | rs398122376 |
hgdp | rs398122376 |
ensembl | rs398122376 |
geneview | rs398122376 |
scholar | rs398122376 |
rs398122376 | |
pharmgkb | rs398122376 |
gwascentral | rs398122376 |
openSNP | rs398122376 |
23andMe | rs398122376 |
SNPshot | rs398122376 |
SNPdbe | rs398122376 |
MSV3d | rs398122376 |
GWAS Ctlg | rs398122376 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs398122376(AAAA;AAAA) |
Alt | rs398122376(AAAA;AAAA) |
Reference | Rs398122376(-;-) |
Significance | Pathogenic |
Disease | Dysgnathia complex |
Variation | info |
Gene | PRRX1 |
CLNDBN | Dysgnathia complex |
Reversed | 0 |
HGVS | NC_000001.10:g.170688891_170688894dupAAAA |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000043530.28, |