rs10061133
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10061133(A;A) |
Make rs10061133(A;G) |
Make rs10061133(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 5 |
Position | 55170716 |
Gene | CDC20B, MIR449A, MIR449B |
is a | snp |
is | mentioned by |
dbSNP | rs10061133 |
dbSNP (classic) | rs10061133 |
ClinGen | rs10061133 |
ebi | rs10061133 |
HLI | rs10061133 |
Exac | rs10061133 |
Gnomad | rs10061133 |
Varsome | rs10061133 |
LitVar | rs10061133 |
Map | rs10061133 |
PheGenI | rs10061133 |
Biobank | rs10061133 |
1000 genomes | rs10061133 |
hgdp | rs10061133 |
ensembl | rs10061133 |
geneview | rs10061133 |
scholar | rs10061133 |
rs10061133 | |
pharmgkb | rs10061133 |
gwascentral | rs10061133 |
openSNP | rs10061133 |
23andMe | rs10061133 |
SNPshot | rs10061133 |
SNPdbe | rs10061133 |
MSV3d | rs10061133 |
GWAS Ctlg | rs10061133 |
Max Magnitude | 0 |
[PMID 27552335] The miR-449b polymorphism, rs10061133 A>G, is associated with premature ovarian insufficiency.