List of variants reported as uncertain significance for endometrial disorder by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.431G>T (p.Ser144Ile)	rs3211299	0.00158
NM_004360.5(CDH1):c.2104G>A (p.Glu702Lys)	rs149127230	0.00058
NM_004360.5(CDH1):c.8C>G (p.Pro3Arg)	rs587782484	0.00023
NM_000179.3(MSH6):c.2426_2428del (p.Val809del)	rs587779240

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