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rs1006113

From SNPedia

Orientationplus
Make rs1006113(A;A)
Make rs1006113(A;G)
Make rs1006113(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position8388584
GeneACOX3
is asnp
is mentioned by
dbSNPrs1006113
ebirs1006113
HLIrs1006113
Exacrs1006113
Varsomers1006113
Maprs1006113
PheGenIrs1006113
hapmaprs1006113
1000 genomesrs1006113
hgdprs1006113
ensemblrs1006113
gopubmedrs1006113
geneviewrs1006113
scholarrs1006113
googlers1006113
pharmgkbrs1006113
gwascentralrs1006113
openSNPrs1006113
23andMers1006113
23andMe allrs1006113
SNP Nexus

SNPshotrs1006113
SNPdbers1006113
MSV3drs1006113
GWAS Ctlgrs1006113
Max Magnitude

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