rs1335292601
This variant is located in the NOBOX gene.
▶ClinVar annotation
About NOBOX
This homeobox gene encodes a transcription factor that is thought to play a role in oogenesis. In mice, it is essential for folliculogenesis and regulation of oocyte-specific genes. Defects in this gene result in premature ovarian failure type 5.[provided by RefSeq, May 2011]
View all NOBOX variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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