List of variants reported as uncertain significance for Cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies by Labcorp Genetics (formerly Invitae), Labcorp

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Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_170675.5(MEIS2):c.1129A>C (p.Met377Leu)	rs534636474	0.00004
NM_170675.5(MEIS2):c.607C>A (p.Leu203Ile)	rs185278462	0.00002
NM_170675.5(MEIS2):c.387+6G>C	rs375137883	0.00001
NM_170675.5(MEIS2):c.505G>A (p.Asp169Asn)	rs1039511168	0.00001
NM_170675.5(MEIS2):c.733G>A (p.Gly245Arg)	rs375357305	0.00001
NM_170675.5(MEIS2):c.1031G>A (p.Arg344Gln)	rs2141225052
NM_170675.5(MEIS2):c.1147+344A>G
NM_170675.5(MEIS2):c.1147+355G>T
NM_170675.5(MEIS2):c.1147+356G>A
NM_170675.5(MEIS2):c.1147+5G>C
NM_170675.5(MEIS2):c.132G>T (p.Pro44=)
NM_170675.5(MEIS2):c.142A>G (p.Thr48Ala)	rs1596139159
NM_170675.5(MEIS2):c.17A>C (p.Asp6Ala)	rs757192671
NM_170675.5(MEIS2):c.445C>G (p.Gln149Glu)
NM_170675.5(MEIS2):c.576_578inv (p.Arg192_Asp193delinsSerLeu)
NM_170675.5(MEIS2):c.904C>A (p.Pro302Thr)
NM_170675.5(MEIS2):c.97A>G (p.Ile33Val)	rs774160502

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