rs12381366
From SNPedia
Merged into | rs9639947 |
Orientation | plus |
Make rs12381366(A;A) |
Make rs12381366(A;G) |
Make rs12381366(G;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 7 |
Position | 46237900 |
Gene | LOC107986792 |
is a | snp |
is | mentioned by |
dbSNP | rs12381366 |
dbSNP (classic) | rs12381366 |
ClinGen | rs12381366 |
ebi | rs12381366 |
HLI | rs12381366 |
Exac | rs12381366 |
Gnomad | rs12381366 |
Varsome | rs12381366 |
LitVar | rs12381366 |
Map | rs12381366 |
PheGenI | rs12381366 |
Biobank | rs12381366 |
1000 genomes | rs12381366 |
hgdp | rs12381366 |
ensembl | rs12381366 |
geneview | rs12381366 |
scholar | rs12381366 |
rs12381366 | |
pharmgkb | rs12381366 |
gwascentral | rs12381366 |
openSNP | rs12381366 |
23andMe | rs12381366 |
SNPshot | rs12381366 |
SNPdbe | rs12381366 |
MSV3d | rs12381366 |
GWAS Ctlg | rs12381366 |
Status | Merged into rs9639947 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 30172247] Association between PTCH1 and RAD54B single-nucleotide polymorphisms and non-syndromic orofacial clefts in a northern Chinese population.