rs937091
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs937091(G;G) |
Make rs937091(G;T) |
Make rs937091(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 119873770 |
is a | snp |
is | mentioned by |
dbSNP | rs937091 |
dbSNP (classic) | rs937091 |
ClinGen | rs937091 |
ebi | rs937091 |
HLI | rs937091 |
Exac | rs937091 |
Gnomad | rs937091 |
Varsome | rs937091 |
LitVar | rs937091 |
Map | rs937091 |
PheGenI | rs937091 |
Biobank | rs937091 |
1000 genomes | rs937091 |
hgdp | rs937091 |
ensembl | rs937091 |
geneview | rs937091 |
scholar | rs937091 |
rs937091 | |
pharmgkb | rs937091 |
gwascentral | rs937091 |
openSNP | rs937091 |
23andMe | rs937091 |
SNPshot | rs937091 |
SNPdbe | rs937091 |
MSV3d | rs937091 |
GWAS Ctlg | rs937091 |
GMAF | 0.4761 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 19200523] Mutations in radial spoke head protein genes RSPH9 and RSPH4A cause primary ciliary dyskinesia with central-microtubular-pair abnormalities.