List of variants reported as likely pathogenic for Lynch syndrome by Mendelics

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000535.7(PMS2):c.137G>T (p.Ser46Ile)	rs121434629	0.00018
NM_000179.3(MSH6):c.1634_1635del (p.Lys545fs)	rs267608064
NM_000179.3(MSH6):c.3018C>A (p.Tyr1006Ter)	rs1553414395
NM_000179.3(MSH6):c.3753_3756dup (p.Val1253fs)	rs876661222
NM_000179.3(MSH6):c.3996_3999dup (p.Arg1334fs)	rs1553333753
NM_000249.4(MLH1):c.1278_1279insTG (p.Gln427fs)	rs1559553492
NM_000249.4(MLH1):c.1387G>T (p.Gly463Ter)	rs1559554339
NM_000249.4(MLH1):c.1864del (p.Ala623fs)	rs1559588540
NM_000249.4(MLH1):c.2262del (p.Arg755fs)	rs267607904
NM_000535.7(PMS2):c.1831dup (p.Ile611fs)	rs63750250

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