rs373900644
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common/normal |
(C;T) | 3 | Carrier of an orofaciodigital mutation |
(T;T) | 9 | Orofaciodigital syndrome likely |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 4 |
Position | 127663438 |
Gene | INTU |
is a | snp |
is | mentioned by |
dbSNP | rs373900644 |
dbSNP (classic) | rs373900644 |
ClinGen | rs373900644 |
ebi | rs373900644 |
HLI | rs373900644 |
Exac | rs373900644 |
Gnomad | rs373900644 |
Varsome | rs373900644 |
LitVar | rs373900644 |
Map | rs373900644 |
PheGenI | rs373900644 |
Biobank | rs373900644 |
1000 genomes | rs373900644 |
hgdp | rs373900644 |
ensembl | rs373900644 |
geneview | rs373900644 |
scholar | rs373900644 |
rs373900644 | |
pharmgkb | rs373900644 |
gwascentral | rs373900644 |
openSNP | rs373900644 |
23andMe | rs373900644 |
SNPshot | rs373900644 |
SNPdbe | rs373900644 |
MSV3d | rs373900644 |
GWAS Ctlg | rs373900644 |
Max Magnitude | 9 |
23andMe calls this i6023169
see [PMID 27158779]