rs150681845
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 9 | Orofaciodigital syndrome likely |
(A;G) | 3 | Carrier of an orofaciodigital mutation |
(G;G) | 0 | common/normal |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 4 |
Position | 127687772 |
Gene | INTU |
is a | snp |
is | mentioned by |
dbSNP | rs150681845 |
dbSNP (classic) | rs150681845 |
ClinGen | rs150681845 |
ebi | rs150681845 |
HLI | rs150681845 |
Exac | rs150681845 |
Gnomad | rs150681845 |
Varsome | rs150681845 |
LitVar | rs150681845 |
Map | rs150681845 |
PheGenI | rs150681845 |
Biobank | rs150681845 |
1000 genomes | rs150681845 |
hgdp | rs150681845 |
ensembl | rs150681845 |
geneview | rs150681845 |
scholar | rs150681845 |
rs150681845 | |
pharmgkb | rs150681845 |
gwascentral | rs150681845 |
openSNP | rs150681845 |
23andMe | rs150681845 |
SNPshot | rs150681845 |
SNPdbe | rs150681845 |
MSV3d | rs150681845 |
GWAS Ctlg | rs150681845 |
Max Magnitude | 9 |
see [PMID 27158779]