List of variants reported as uncertain significance for Familial adenomatous polyposis 2; Pilomatrixoma; Neoplasm of stomach by Fulgent Genetics, Fulgent Genetics

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001048174.2(MUTYH):c.848G>A (p.Arg283Lys)	rs149342980	0.00021
NM_001048174.2(MUTYH):c.1171G>A (p.Ala391Thr)	rs587780744	0.00009
NM_001048174.2(MUTYH):c.901G>A (p.Val301Met)	rs147718169	0.00008
NM_001048174.2(MUTYH):c.488G>A (p.Arg163Gln)	rs369677603	0.00006
NM_001048174.2(MUTYH):c.1336C>T (p.Arg446Cys)	rs200229669	0.00004
NM_001048174.2(MUTYH):c.263G>A (p.Arg88Gln)	rs587782683	0.00003
NM_001048174.2(MUTYH):c.916C>G (p.Pro306Ala)	rs587778537	0.00002
NM_001048174.2(MUTYH):c.1409A>G (p.Gln470Arg)	rs587780085	0.00001

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