rs5995288
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs5995288(C;C) |
Make rs5995288(C;T) |
Make rs5995288(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 36366589 |
Gene | MYH9 |
is a | snp |
is | mentioned by |
dbSNP | rs5995288 |
dbSNP (classic) | rs5995288 |
ClinGen | rs5995288 |
ebi | rs5995288 |
HLI | rs5995288 |
Exac | rs5995288 |
Gnomad | rs5995288 |
Varsome | rs5995288 |
LitVar | rs5995288 |
Map | rs5995288 |
PheGenI | rs5995288 |
Biobank | rs5995288 |
1000 genomes | rs5995288 |
hgdp | rs5995288 |
ensembl | rs5995288 |
geneview | rs5995288 |
scholar | rs5995288 |
rs5995288 | |
pharmgkb | rs5995288 |
gwascentral | rs5995288 |
openSNP | rs5995288 |
23andMe | rs5995288 |
SNPshot | rs5995288 |
SNPdbe | rs5995288 |
MSV3d | rs5995288 |
GWAS Ctlg | rs5995288 |
GMAF | 0.4784 |
Max Magnitude | 0 |
[PMID 19320731] Further evidence for the involvement of MYH9 in the etiology of non-syndromic cleft lip with or without cleft palate
[PMID 18716610] Genomic screening identifies novel linkages and provides further evidence for a role of MYH9 in nonsyndromic cleft lip and palate.