List of variants reported as likely benign for Lynch syndrome 4 by Myriad Genetics, Inc.

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Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_000535.7(PMS2):c.2350G>A (p.Asp784Asn)	rs143340522	0.00192
NM_000535.7(PMS2):c.2149G>A (p.Val717Met)	rs201671325	0.00072
NM_000535.7(PMS2):c.936G>A (p.Met312Ile)	rs139194813	0.00041
NM_000535.7(PMS2):c.857A>G (p.Asp286Gly)	rs116788608	0.00011
NM_000535.7(PMS2):c.2276-10A>G	rs573900018	0.00010
NM_000535.7(PMS2):c.1714G>A (p.Ala572Thr)	rs63751023	0.00009
NM_000535.7(PMS2):c.353+6A>G	rs376449640	0.00006
NM_000535.7(PMS2):c.166C>G (p.Leu56Val)	rs371011390	0.00004
NM_000535.7(PMS2):c.2356C>A (p.Leu786Met)	rs576055272	0.00004
NM_000535.7(PMS2):c.1096G>C (p.Asp366His)	rs141769057	0.00003
NM_000535.7(PMS2):c.598G>A (p.Val200Ile)	rs587778620	0.00002
NM_000535.7(PMS2):c.1240G>T (p.Asp414Tyr)	rs370752614	0.00001
NM_000535.7(PMS2):c.354-7C>T	rs758471869	0.00001
NM_000535.7(PMS2):c.880C>T (p.Arg294Trp)	rs563433235	0.00001
NM_000535.7(PMS2):c.983A>G (p.Asp328Gly)	rs587782852	0.00001
NM_000535.7(PMS2):c.1393A>C (p.Lys465Gln)	rs1060503135
NM_000535.7(PMS2):c.2175-11G>T	rs538914402
NM_000535.7(PMS2):c.23+6C>T	rs779104357
NM_000535.7(PMS2):c.804-12A>G	rs1221537446

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