Paget Disease of Bone 2

Other 82 variants 2 genes

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Associated Genes (2)

SQSTM1 TNFRSF11A

Associated Variants (82)

RSID	Gene	Risk Allele	Odds Ratio	Evidence
RS2480264648	SQSTM1	—	—	strong
RS765610848	SQSTM1	—	—	strong
RS2113487920	SQSTM1	—	—	strong
RS2113512370	SQSTM1	—	—	strong
RS1391182750	SQSTM1	—	—	strong
RS143511494	SQSTM1	—	—	strong
RS2113485289	SQSTM1	—	—	strong
RS766330561	TNFRSF11A	—	—	strong
RS202235745	SQSTM1	—	—	strong
RS771657338	SQSTM1	—	—	strong
RS2480264715	SQSTM1	—	—	strong
RS1258386028	SQSTM1	—	—	strong
RS1166729262	SQSTM1	—	—	strong
RS201923000	SQSTM1	—	—	strong
RS2480244186	SQSTM1	—	—	strong
RS2480208932	SQSTM1	—	—	strong
RS2113512406	SQSTM1	—	—	strong
RS1757759029	SQSTM1	—	—	strong
RS2480244231	SQSTM1	—	—	strong
RS373306317	SQSTM1	—	—	strong
RS2480199584	SQSTM1	—	—	strong
RS1261101487	SQSTM1	—	—	strong
RS2480243842	SQSTM1	—	—	strong
RS1758351897	SQSTM1	—	—	strong
RS1008679317	SQSTM1	—	—	strong
RS372772575	TNFRSF11A	—	—	strong
RS140341924	SQSTM1	—	—	strong
RS762733251	TNFRSF11A	—	—	strong
RS138204772	TNFRSF11A	—	—	strong
RS145242277	TNFRSF11A	—	—	strong
RS149842577	TNFRSF11A	—	—	strong
RS200952751	TNFRSF11A	—	—	strong
RS141436407	SQSTM1	—	—	strong
RS143956614	SQSTM1	—	—	strong
RS369418441	TNFRSF11A	—	—	strong
RS376113816	TNFRSF11A	—	—	strong
RS572639953	TNFRSF11A	—	—	strong
RS761709562	TNFRSF11A	—	—	strong
RS34966542	TNFRSF11A	—	—	strong
RS775988188	SQSTM1	—	—	strong
RS771036207	SQSTM1	—	—	strong
RS1758316662	SQSTM1	—	—	strong
RS1757883398	SQSTM1	—	—	strong
RS1302810798	SQSTM1	—	—	strong
RS1425863340	SQSTM1	—	—	strong
RS1758558921	SQSTM1	—	—	strong
RS771966860	SQSTM1	—	—	strong
RS143746604	SQSTM1	—	—	strong
RS535606152	SQSTM1	—	—	strong
RS757212984	SQSTM1	—	—	strong

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