rs34201045
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs34201045(-;-) |
Make rs34201045(-;AG) |
Make rs34201045(AG;AG) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 189789729 |
Gene | TP63 |
is a | snp |
is | mentioned by |
dbSNP | rs34201045 |
dbSNP (classic) | rs34201045 |
ClinGen | rs34201045 |
ebi | rs34201045 |
HLI | rs34201045 |
Exac | rs34201045 |
Gnomad | rs34201045 |
Varsome | rs34201045 |
LitVar | rs34201045 |
Map | rs34201045 |
PheGenI | rs34201045 |
Biobank | rs34201045 |
1000 genomes | rs34201045 |
hgdp | rs34201045 |
ensembl | rs34201045 |
geneview | rs34201045 |
scholar | rs34201045 |
rs34201045 | |
pharmgkb | rs34201045 |
gwascentral | rs34201045 |
openSNP | rs34201045 |
23andMe | rs34201045 |
SNPshot | rs34201045 |
SNPdbe | rs34201045 |
MSV3d | rs34201045 |
GWAS Ctlg | rs34201045 |
Max Magnitude | 0 |
[PMID 18515319] Homozygous WNT10b mutation and complex inheritance in Split-Hand/Foot Malformation.