rs200649783
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 9 | Orofaciodigital syndrome likely |
(A;C) | 3 | Carrier of an orofaciodigital mutation |
(C;C) | 0 | common/normal |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 2 |
Position | 19969556 |
Gene | WDR35 |
is a | snp |
is | mentioned by |
dbSNP | rs200649783 |
dbSNP (classic) | rs200649783 |
ClinGen | rs200649783 |
ebi | rs200649783 |
HLI | rs200649783 |
Exac | rs200649783 |
Gnomad | rs200649783 |
Varsome | rs200649783 |
LitVar | rs200649783 |
Map | rs200649783 |
PheGenI | rs200649783 |
Biobank | rs200649783 |
1000 genomes | rs200649783 |
hgdp | rs200649783 |
ensembl | rs200649783 |
geneview | rs200649783 |
scholar | rs200649783 |
rs200649783 | |
pharmgkb | rs200649783 |
gwascentral | rs200649783 |
openSNP | rs200649783 |
23andMe | rs200649783 |
SNPshot | rs200649783 |
SNPdbe | rs200649783 |
MSV3d | rs200649783 |
GWAS Ctlg | rs200649783 |
Max Magnitude | 9 |
see [PMID 27158779]