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rs10061133

From SNPedia

Orientationplus
Make rs10061133(A;A)
Make rs10061133(A;G)
Make rs10061133(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position55170716
GeneCDC20B, MIR449A, MIR449B
is asnp
is mentioned by
dbSNPrs10061133
ebirs10061133
HLIrs10061133
Exacrs10061133
Varsomers10061133
Maprs10061133
PheGenIrs10061133
hapmaprs10061133
1000 genomesrs10061133
hgdprs10061133
ensemblrs10061133
gopubmedrs10061133
geneviewrs10061133
scholarrs10061133
googlers10061133
pharmgkbrs10061133
gwascentralrs10061133
openSNPrs10061133
23andMers10061133
23andMe allrs10061133
SNP Nexus

SNPshotrs10061133
SNPdbers10061133
MSV3drs10061133
GWAS Ctlgrs10061133
Max Magnitude

[PMID 27552335] The miR-449b polymorphism, rs10061133 A>G, is associated with premature ovarian insufficiency.