Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia

Neurological 48 variants 1 gene

Upload your DNA to see your personal risk score for Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia.

Associated Genes (1)

VCP

Associated Variants (48)

RSID	Gene	Risk Allele	Odds Ratio	Evidence
RS1828865320	VCP	—	—	strong
RS1563976866	VCP	—	—	strong
RS758169026	VCP	—	—	strong
RS549915384	VCP	—	—	strong
RS201610567	VCP	—	—	strong
RS751290466	VCP	—	—	strong
RS921092914	VCP	—	—	strong
RS1828783140	VCP	—	—	strong
RS1554668814	VCP	—	—	strong
RS367703031	VCP	—	—	strong
RS370700002	VCP	—	—	strong
RS1828723406	VCP	—	—	strong
RS375262833	VCP	—	—	strong
RS1828784075	VCP	—	—	strong
RS541980846	VCP	—	—	strong
RS1563981227	VCP	—	—	strong
RS767379602	VCP	—	—	strong
RS1563980966	VCP	—	—	strong
RS1554668813	VCP	—	—	strong
RS1260699314	VCP	—	—	strong
RS1554668817	VCP	—	—	strong
RS774809989	VCP	—	—	strong
RS2490370338	VCP	—	—	strong
RS900105227	VCP	—	—	strong
RS1554668979	VCP	—	—	strong
RS121909330	VCP	—	—	strong
RS121909332	VCP	—	—	strong
RS121909334	VCP	—	—	strong
RS121909335	VCP	—	—	strong
RS387906789	VCP	—	—	strong
RS863225291	VCP	—	—	strong
RS864309501	VCP	—	—	strong
RS864309502	VCP	—	—	strong
RS147623367	VCP	—	—	strong
RS377316335	VCP	—	—	strong
RS370296303	VCP	—	—	strong
RS121909329	VCP	—	—	strong
RS779959657	VCP	—	—	strong
RS577812326	VCP	—	—	strong
RS148329626	VCP	—	—	strong
RS141275388	VCP	—	—	strong
RS1554668168	VCP	—	—	strong
RS1554668805	VCP	—	—	strong
RS183223259	VCP	—	—	strong
RS1563980403	VCP	—	—	strong
RS1554669087	VCP	—	—	strong
RS376510669	VCP	—	—	strong
RS1563980979	VCP	—	—	strong