rs10787738
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10787738(C;C) |
Make rs10787738(C;T) |
Make rs10787738(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 117017860 |
Gene | SHTN1 |
is a | snp |
is | mentioned by |
dbSNP | rs10787738 |
dbSNP (classic) | rs10787738 |
ClinGen | rs10787738 |
ebi | rs10787738 |
HLI | rs10787738 |
Exac | rs10787738 |
Gnomad | rs10787738 |
Varsome | rs10787738 |
LitVar | rs10787738 |
Map | rs10787738 |
PheGenI | rs10787738 |
Biobank | rs10787738 |
1000 genomes | rs10787738 |
hgdp | rs10787738 |
ensembl | rs10787738 |
geneview | rs10787738 |
scholar | rs10787738 |
rs10787738 | |
pharmgkb | rs10787738 |
gwascentral | rs10787738 |
openSNP | rs10787738 |
23andMe | rs10787738 |
SNPshot | rs10787738 |
SNPdbe | rs10787738 |
MSV3d | rs10787738 |
GWAS Ctlg | rs10787738 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 25099202] Genetic risk factors for orofacial clefts in Central Africans and Southeast Asians