rs2032582 is a genetic variant on gene ABCB1 associated with Inflammatory bowel disease 13.
rs10876864 is a genetic variant on gene IKZF4 associated with Intelligence and Allergic disease.
rs11540652 is a genetic variant on gene TP53 associated with Li-fraumeni syndrome 1 and Multiple myeloma.
rs104894226 is a genetic variant on gene HRAS associated with Costello syndrome and Large congenital melanocytic nevus.
rs7274581 is a genetic variant associated with Alzheimer's disease.
rs10808546 is a genetic variant associated with Abdominal aortic aneurysm.
is a rare inherited condition causing developmental delay and intellectual disability.
is a rare autosomal recessive condition causing developmental and intellectual disabilities.
is a rare autosomal recessive condition causing developmental delay and intellectual disability.
is a rare autosomal recessive condition causing developmental delays and intellectual disability.
is an autosomal recessive disorder causing developmental delay and intellectual disability.
is a rare autosomal recessive disorder causing developmental and intellectual disabilities.
is an inherited (autosomal recessive) condition causing developmental delays and intellectual disability.
is a rare inherited condition causing developmental delays and intellectual disability.
is a rare autosomal recessive condition causing lifelong learning and developmental challenges.
is a rare inherited disorder causing developmental delays and intellectual disability.
is rare inherited (autosomal recessive), causing developmental delays and learning disability.
is a rare inherited condition causing developmental delays and lifelong learning difficulties.
is a rare autosomal recessive disorder causing developmental delay and intellectual disability.
is a rare genetic disorder causing developmental delays and intellectual disability.
is a rare autosomal recessive disorder causing developmental and intellectual delays.
is a rare genetic condition causing developmental delays and intellectual disability.
is an autosomal recessive disorder causing developmental delays and intellectual disability.
is a rare autosomal-recessive condition causing developmental delay and intellectual disability.
