List of variants reported as likely benign for Familial adenomatous polyposis 2 by Counsyl

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Total variants: 30

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HGVS	dbSNP	gnomAD frequency
NM_001048174.2(MUTYH):c.914-27G>A	rs188830619	0.00113
NM_001048174.2(MUTYH):c.1102+9A>T	rs587780742	0.00018
NM_001048174.2(MUTYH):c.420+16G>A	rs576152721	0.00018
NM_001128425.2(MUTYH):c.42C>T (p.Ile14=)	rs202240122	0.00017
NM_001048174.2(MUTYH):c.1393-17C>G	rs199664013	0.00012
NM_001048174.2(MUTYH):c.1034C>T (p.Ala345Val)	rs35352891	0.00011
NM_001048174.2(MUTYH):c.132G>A (p.Pro44=)	rs144551668	0.00011
NM_001048174.2(MUTYH):c.-6-7G>A	rs780029247	0.00010
NM_001048174.2(MUTYH):c.612C>T (p.Thr204=)	rs780747266	0.00009
NM_001048174.2(MUTYH):c.21C>T (p.Ala7=)	rs201982344	0.00007
NM_001048174.2(MUTYH):c.729C>T (p.Asp243=)	rs730881838	0.00006
NM_001048174.2(MUTYH):c.630C>T (p.Asn210=)	rs767327888	0.00005
NM_001048174.2(MUTYH):c.1062C>T (p.Ala354=)	rs778193554	0.00004
NM_001048174.2(MUTYH):c.87C>T (p.Asn29=)	rs141679570	0.00004
NM_001048174.2(MUTYH):c.900C>T (p.Asp300=)	rs587780752	0.00003
NM_001048174.2(MUTYH):c.914-21T>C	rs780013757	0.00003
NM_001048174.2(MUTYH):c.441T>C (p.Ala147=)	rs786201352	0.00002
NM_001048174.2(MUTYH):c.1227G>A (p.Arg409=)	rs199575659	0.00001
NM_001048174.2(MUTYH):c.1311A>C (p.Pro437=)	rs768239149	0.00001
NM_001048174.2(MUTYH):c.138G>A (p.Glu46=)	rs376861118	0.00001
NM_001048174.2(MUTYH):c.288C>T (p.Asp96=)	rs730881836	0.00001
NM_001048174.2(MUTYH):c.305-7C>A	rs863224698	0.00001
NM_001048174.2(MUTYH):c.492+20G>A	rs776504435	0.00001
NM_001048174.2(MUTYH):c.798C>T (p.Arg266=)	rs587780750	0.00001
NM_001048174.2(MUTYH):c.802C>T (p.Leu268=)	rs778782508	0.00001
NM_001048174.2(MUTYH):c.914-8G>A	rs757672024	0.00001
NM_001048174.2(MUTYH):c.1435-9T>C	rs372815910
NM_001048174.2(MUTYH):c.282C>T (p.Asp94=)	rs876660505
NM_001048174.2(MUTYH):c.327G>A (p.Leu109=)	rs1057517458
NM_001128425.2(MUTYH):c.36+20C>G	rs540793556

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