rs9619601
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9619601(A;A) |
Make rs9619601(A;G) |
Make rs9619601(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 22 |
Position | 36304129 |
Gene | MYH9 |
is a | snp |
is | mentioned by |
dbSNP | rs9619601 |
dbSNP (classic) | rs9619601 |
ClinGen | rs9619601 |
ebi | rs9619601 |
HLI | rs9619601 |
Exac | rs9619601 |
Gnomad | rs9619601 |
Varsome | rs9619601 |
LitVar | rs9619601 |
Map | rs9619601 |
PheGenI | rs9619601 |
Biobank | rs9619601 |
1000 genomes | rs9619601 |
hgdp | rs9619601 |
ensembl | rs9619601 |
geneview | rs9619601 |
scholar | rs9619601 |
rs9619601 | |
pharmgkb | rs9619601 |
gwascentral | rs9619601 |
openSNP | rs9619601 |
23andMe | rs9619601 |
SNPshot | rs9619601 |
SNPdbe | rs9619601 |
MSV3d | rs9619601 |
GWAS Ctlg | rs9619601 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 29207917] Functional Effects of SNPs in MYH9 and Risks of Nonsyndromic Orofacial Clefts.