List of variants reported as likely benign for Multiple endocrine neoplasia by Illumina Laboratory Services, Illumina

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Total variants: 33

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HGVS	dbSNP	gnomAD frequency
NM_020975.5(RET):c.-196C>A	rs10900297	0.41632
NM_020975.6(RET):c.337+9G>A	rs2435351	0.20641
NM_020975.6(RET):c.2071G>A (p.Gly691Ser)	rs1799939	0.16640
NM_020975.6(RET):c.*1969T>C	rs3026785	0.04255
NM_020975.6(RET):c.2508C>T (p.Ser836=)	rs1800862	0.03791
NM_020975.6(RET):c.1264-5C>T	rs9282835	0.02749
NM_020975.6(RET):c.2944C>T (p.Arg982Cys)	rs17158558	0.01567
NM_020975.6(RET):c.*1742G>A	rs143369221	0.00349
NM_020975.6(RET):c.337+12G>A	rs200468424	0.00198
NM_020975.6(RET):c.2372A>T (p.Tyr791Phe)	rs77724903	0.00178
NM_004064.5(CDKN1B):c.475+10C>T	rs36101844	0.00096
NM_020975.6(RET):c.200G>A (p.Arg67His)	rs192489011	0.00036
NM_020975.6(RET):c.2088G>A (p.Ser696=)	rs150329150	0.00024
NM_020975.6(RET):c.785T>C (p.Val262Ala)	rs139790943	0.00024
NM_020975.6(RET):c.874G>A (p.Val292Met)	rs34682185	0.00023
NM_020975.6(RET):c.*84G>A	rs558718557	0.00022
NM_020975.6(RET):c.1063+9G>A	rs765463636	0.00014
NM_020975.6(RET):c.2988G>A (p.Pro996=)	rs145798106	0.00014
NM_020975.6(RET):c.2081G>A (p.Arg694Gln)	rs141185224	0.00008
NM_004064.5(CDKN1B):c.*327C>T	rs529020970	0.00006
NM_020975.6(RET):c.1118C>T (p.Ala373Val)	rs546866208	0.00004
NM_020975.6(RET):c.3253A>G (p.Thr1085Ala)	rs756465544	0.00004
NM_020975.6(RET):c.718G>C (p.Val240Leu)	rs375120544	0.00004
NM_020975.6(RET):c.972G>C (p.Trp324Cys)	rs758298916	0.00003
NM_020975.6(RET):c.1920C>T (p.Ala640=)	rs149768519	0.00002
NM_004064.4(CDKN1B):c.*1357T>C	rs530782147	0.00001
NM_020975.6(RET):c.2070C>T (p.Ser690=)	rs201550433	0.00001
NM_020975.6(RET):c.2538C>T (p.Leu846=)	rs201816539	0.00001
NM_020975.6(RET):c.3052C>T (p.Leu1018Phe)	rs766330880	0.00001
NM_001370259.2(MEN1):c.*300CTC[2]	rs143341556
NM_004064.5(CDKN1B):c.-31AG[1]	rs774454456
NM_020975.6(RET):c.*499dup	rs201945709
NM_020975.6(RET):c.566G>A (p.Arg189His)	rs753707182

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