List of variants in gene RET reported as uncertain significance for Familial medullary thyroid carcinoma

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.1699G>A (p.Asp567Asn)	rs147219360	0.00014
NM_020975.6(RET):c.604G>A (p.Val202Met)	rs751572082	0.00006
NM_020975.6(RET):c.539G>A (p.Arg180Gln)	rs370736139	0.00003
NM_020975.6(RET):c.3200C>T (p.Pro1067Leu)	rs760625882	0.00002
NM_020975.6(RET):c.1921G>A (p.Ala641Thr)	rs377767411	0.00001
NM_020975.6(RET):c.431G>A (p.Arg144His)	rs551142665	0.00001
NM_020975.6(RET):c.530G>A (p.Arg177Gln)	rs759229505	0.00001
NM_020975.6(RET):c.701G>A (p.Arg234Gln)	rs756216318	0.00001
NM_020975.6(RET):c.1232C>G (p.Ser411Cys)	rs2132746693
NM_020975.6(RET):c.1921G>C (p.Ala641Pro)	rs377767411
NM_020975.6(RET):c.1942G>T (p.Val648Phe)	rs77711105
NM_020975.6(RET):c.2330A>G (p.Asn777Ser)	rs377767415
NM_020975.6(RET):c.2531G>A (p.Arg844Gln)	rs55947360
NM_020975.6(RET):c.3137C>A (p.Ala1046Asp)	rs945693739

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