rs78950893
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs78950893(C;C) |
Make rs78950893(C;T) |
Make rs78950893(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 18 |
Position | 48942348 |
Gene | SMAD7 |
is a | snp |
is | mentioned by |
dbSNP | rs78950893 |
dbSNP (classic) | rs78950893 |
ClinGen | rs78950893 |
ebi | rs78950893 |
HLI | rs78950893 |
Exac | rs78950893 |
Gnomad | rs78950893 |
Varsome | rs78950893 |
LitVar | rs78950893 |
Map | rs78950893 |
PheGenI | rs78950893 |
Biobank | rs78950893 |
1000 genomes | rs78950893 |
hgdp | rs78950893 |
ensembl | rs78950893 |
geneview | rs78950893 |
scholar | rs78950893 |
rs78950893 | |
pharmgkb | rs78950893 |
gwascentral | rs78950893 |
openSNP | rs78950893 |
23andMe | rs78950893 |
SNPshot | rs78950893 |
SNPdbe | rs78950893 |
MSV3d | rs78950893 |
GWAS Ctlg | rs78950893 |
Max Magnitude | 0 |
[PMID 27242896] Fine-Mapping of 18q21.1 Locus Identifies Single Nucleotide Polymorphisms Associated with Nonsyndromic Cleft Lip with or without Cleft Palate.