QRICH2 Chromosome 17

Glutamine rich 2
9 variants 9 Health Risk

Upload your DNA to see your personal genotypes for variants in QRICH2.

What This Gene Does
Involved in cell projection assembly; flagellated sperm motility; and negative regulation of ubiquitin-dependent protein catabolic process. Located in sperm flagellum. Implicated in spermatogenic failure 35. [provided by Alliance of Genome Resources, Jul 2025]
Associated Conditions (2)
QRICH2-related disorder
Spermatogenic failure 35
Key Variants
All Variants (9)
RSID Category Clinical Significance Conditions
RS148370256 Health Risk Conflicting classifications of pathogenicity QRICH2-related disorder, QRICH2-related disorder
RS186517232 Health Risk Conflicting classifications of pathogenicity
RS555028656 Health Risk Conflicting classifications of pathogenicity Spermatogenic failure 35, Spermatogenic failure 35
RS1161756211 Health Risk Likely pathogenic QRICH2-related disorder, QRICH2-related disorder
RS2143116895 Health Risk Likely pathogenic
RS1567790522 Health Risk Pathogenic Spermatogenic failure 35, Spermatogenic failure 35
RS770382841 Health Risk Pathogenic Spermatogenic failure 35, Spermatogenic failure 35
RS777214459 Health Risk Pathogenic Spermatogenic failure 35, Spermatogenic failure 35
RS934388592 Health Risk Pathogenic Spermatogenic failure 35, Spermatogenic failure 35
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