Mitochondrial Myopathy-cerebellar Ataxia-pigmentary Retinopathy Syndrome

Other 17 variants 1 gene

Upload your DNA to see your personal risk score for Mitochondrial Myopathy-cerebellar Ataxia-pigmentary Retinopathy Syndrome.

Associated Genes (1)

MSTO1

Associated Variants (17)

RSID	Gene	Risk Allele	Odds Ratio	Evidence
RS776826330	MSTO1	—	—	strong
RS764871960	MSTO1	—	—	strong
RS1187504822	MSTO1	—	—	strong
RS1674934230	MSTO1	—	—	strong
RS767313156	MSTO1	—	—	strong
RS1673545403	MSTO1	—	—	strong
RS745944305	MSTO1	—	—	strong
RS752022363	MSTO1	—	—	strong
RS753488873	MSTO1	—	—	strong
RS749922789	MSTO1	—	—	strong
RS563943670	MSTO1	—	—	strong
RS1208636573	MSTO1	—	—	strong
RS1248439783	MSTO1	—	—	strong
RS762798018	MSTO1	—	—	strong
RS771965165	MSTO1	—	—	strong
RS622288	MSTO1	—	—	strong
RS1553295536	MSTO1	—	—	strong