List of variants reported as likely benign for Arthrogryposis multiplex congenita

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_003282.4(TNNI2):c.60T>C (p.Ser20=)	rs907610	0.82025
NM_002470.4(MYH3):c.5457+9dup	rs397750512	0.58793
NM_003289.4(TPM2):c.773-4_773-3insA	rs1554658501	0.02101
NM_006757.4(TNNT3):c.367-9T>C	rs76471485	0.00859
NM_006757.3(TNNT3):c.-83G>A	rs114407235	0.00585
NM_006757.4(TNNT3):c.414G>A (p.Glu138=)	rs2292470	0.00576
NM_006757.4(TNNT3):c.723-15G>C	rs143255528	0.00407
NM_003282.4(TNNI2):c.*94C>T	rs117830156	0.00349
NM_006757.4(TNNT3):c.*36C>T	rs147535560	0.00188
NM_012243.3(SLC35A3):c.63T>G (p.Val21=)	rs141542767	0.00038
NM_012243.3(SLC35A3):c.348G>A (p.Thr116=)	rs574333514	0.00006
NM_002470.4(MYH3):c.1960-17dup	rs3216884
NM_002470.4(MYH3):c.1960-8del	rs3216884
NM_003289.4(TPM2):c.773-3dup	rs35401252

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