rs781614640

This variant is located in the SMC1B gene.

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ClinVar annotation

Likely Pathogenic

1 submitter

Genetic non-acquired premature ovarian failure

About SMC1B

SMC1L2 belongs to a family of proteins required for chromatid cohesion and DNA recombination during meiosis and mitosis (3:Revenkova et al., 2001 [PubMed 11564881]).[supplied by OMIM, Mar 2008]

View all SMC1B variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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