MEIOB Chromosome 16

Meiosis specific with OB-fold
10 variants 10 Health Risk

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What This Gene Does
Predicted to enable chromatin binding activity; single-stranded DNA 3'-5' DNA exonuclease activity; and single-stranded DNA binding activity. Predicted to be involved in double-strand break repair via homologous recombination; fertilization; and meiotic nuclear division. Located in nucleus. Implicated in primary ovarian insufficiency and spermatogenic failure 22. [provided by Alliance of Genome Resources, Jul 2025]
Associated Conditions (3)
Spermatogenic failure 22
Premature ovarian failure 23
Azoospermia
Key Variants
All Variants (10)
RSID Category Clinical Significance Conditions
RS779513355 Health Risk Likely pathogenic Spermatogenic failure 22, Premature ovarian failure 23, Spermatogenic failure 22
RS972548876 Health Risk Likely pathogenic
RS1010446295 Health Risk Pathogenic Premature ovarian failure 23, Premature ovarian failure 23
RS1555472691 Health Risk Pathogenic Spermatogenic failure 22, Spermatogenic failure 22
RS1899342578 Health Risk Pathogenic Spermatogenic failure 22, Spermatogenic failure 22
RS2142076836 Health Risk Pathogenic Azoospermia, Azoospermia
RS2548195978 Health Risk Pathogenic Spermatogenic failure 22, Spermatogenic failure 22
RS35694423 Health Risk Pathogenic Premature ovarian failure 23, Spermatogenic failure 22, Premature ovarian failure 23
RS745502213 Health Risk Pathogenic
RS750376392 Health Risk Pathogenic Spermatogenic failure 22, Premature ovarian failure 23, Spermatogenic failure 22
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