List of variants reported as likely benign for Multiple endocrine neoplasia type 2A

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 93

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.1336G>C (p.Gly446Arg)	rs115423919	0.00238
NM_020975.6(RET):c.337+12G>A	rs200468424	0.00198
NM_020975.6(RET):c.2372A>T (p.Tyr791Phe)	rs77724903	0.00178
NM_020975.6(RET):c.1197G>A (p.Pro399=)	rs148371113	0.00108
NM_020975.6(RET):c.262A>G (p.Ile88Val)	rs141679950	0.00056
NM_020975.6(RET):c.225G>A (p.Thr75=)	rs151267865	0.00052
NM_020975.6(RET):c.3112A>G (p.Thr1038Ala)	rs201740483	0.00047
NM_020975.6(RET):c.1946C>T (p.Ser649Leu)	rs148935214	0.00039
NM_020975.6(RET):c.200G>A (p.Arg67His)	rs192489011	0.00036
NM_020975.6(RET):c.1158G>A (p.Ala386=)	rs373540097	0.00034
NM_020975.6(RET):c.785T>C (p.Val262Ala)	rs139790943	0.00024
NM_020975.6(RET):c.337+34C>T	rs368088467	0.00022
NM_020975.6(RET):c.73+9278G>A	rs537638504	0.00019
NM_020975.6(RET):c.1531G>A (p.Glu511Lys)	rs201553718	0.00018
NM_020975.6(RET):c.2522C>T (p.Pro841Leu)	rs149891333	0.00015
NM_020975.6(RET):c.1017G>A (p.Ser339=)	rs369810881	0.00014
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.1893C>T (p.Asp631=)	rs55846256	0.00013
NM_020975.6(RET):c.1437C>T (p.Ala479=)	rs576806356	0.00011
NM_020975.6(RET):c.1522+35C>T	rs377130948	0.00011
NM_020975.6(RET):c.1642G>A (p.Gly548Ser)	rs374461212	0.00011
NM_020975.6(RET):c.2556C>G (p.Ile852Met)	rs377767426	0.00011
NM_020975.6(RET):c.2601G>T (p.Glu867Asp)	rs141459368	0.00011
NM_020975.6(RET):c.337+11C>T	rs754967305	0.00011
NM_020975.6(RET):c.1879+17C>T	rs369920430	0.00010
NM_020975.6(RET):c.3243T>C (p.Asp1081=)	rs144192900	0.00010
NM_020975.6(RET):c.1530C>T (p.Ala510=)	rs553492964	0.00009
NM_020975.6(RET):c.1880-13C>A	rs948277023	0.00009
NM_020975.6(RET):c.2136+15G>A	rs751183869	0.00009
NM_020975.6(RET):c.2657G>A (p.Arg886Gln)	rs373594744	0.00009
NM_020975.6(RET):c.1879+13C>T	rs375573788	0.00008
NM_020975.6(RET):c.2081G>A (p.Arg694Gln)	rs141185224	0.00008
NM_020975.6(RET):c.2611G>A (p.Val871Ile)	rs145170911	0.00008
NM_020975.6(RET):c.1182C>T (p.Asn394=)	rs376465385	0.00007
NM_020975.6(RET):c.1942G>A (p.Val648Ile)	rs77711105	0.00007
NM_020975.6(RET):c.1597G>A (p.Gly533Ser)	rs75873440	0.00006
NM_020975.6(RET):c.1649-4G>A	rs369769303	0.00006
NM_020975.6(RET):c.1894G>A (p.Glu632Lys)	rs377767407	0.00006
NM_020975.6(RET):c.2116G>A (p.Val706Met)	rs137855422	0.00006
NM_020975.6(RET):c.2409C>T (p.Ile803=)	rs535051804	0.00006
NM_020975.6(RET):c.337+29G>A	rs578158807	0.00005
NM_020975.6(RET):c.1118C>T (p.Ala373Val)	rs546866208	0.00004
NM_020975.6(RET):c.1891G>A (p.Asp631Asn)	rs377767406	0.00004
NM_020975.6(RET):c.2001A>T (p.Pro667=)	rs563316790	0.00004
NM_020975.6(RET):c.2371T>A (p.Tyr791Asn)	rs377767417	0.00004
NM_020975.6(RET):c.2477A>C (p.Tyr826Ser)	rs34617196	0.00004
NM_020975.6(RET):c.693C>T (p.Arg231=)	rs576806329	0.00004
NM_020975.6(RET):c.1063A>G (p.Arg355Gly)	rs145402131	0.00003
NM_020975.6(RET):c.1760-12G>A	rs377767392	0.00003
NM_020975.6(RET):c.1867G>A (p.Glu623Lys)	rs377767402	0.00003
NM_020975.6(RET):c.1878G>A (p.Gln626=)	rs147692872	0.00003
NM_020975.6(RET):c.1879+14G>A	rs532810255	0.00003
NM_020975.6(RET):c.2285-4T>G	rs376601566	0.00003
NM_020975.6(RET):c.2298G>A (p.Pro766=)	rs140658743	0.00003
NM_020975.6(RET):c.1095G>A (p.Ser365=)	rs201992974	0.00002
NM_020975.6(RET):c.1188G>A (p.Ser396=)	rs758510657	0.00002
NM_020975.6(RET):c.1264-4C>T	rs587780806	0.00002
NM_020975.6(RET):c.2041C>G (p.Gln681Glu)	rs567241943	0.00002
NM_020975.6(RET):c.2226G>A (p.Thr742=)	rs762876946	0.00002
NM_020975.6(RET):c.2393-9C>T	rs567543719	0.00002
NM_020975.6(RET):c.2488G>A (p.Gly830Arg)	rs200127630	0.00002
NM_020975.6(RET):c.1008C>G (p.Asn336Lys)	rs144981275	0.00001
NM_020975.6(RET):c.1052T>A (p.Val351Glu)	rs749449032	0.00001
NM_020975.6(RET):c.1574G>A (p.Arg525Gln)	rs752830820	0.00001
NM_020975.6(RET):c.1618A>G (p.Arg540Gly)	rs543376293	0.00001
NM_020975.6(RET):c.1648+24G>A	rs1057517640	0.00001
NM_020975.6(RET):c.1915G>A (p.Ala639Thr)	rs777122776	0.00001
NM_020975.6(RET):c.1921G>A (p.Ala641Thr)	rs377767411	0.00001
NM_020975.6(RET):c.2070C>T (p.Ser690=)	rs201550433	0.00001
NM_020975.6(RET):c.2289C>T (p.Asn763=)	rs777349208	0.00001
NM_020975.6(RET):c.2365A>G (p.Lys789Glu)	rs1352006130	0.00001
NM_020975.6(RET):c.2715C>T (p.Tyr905=)	rs755023496	0.00001
NM_020975.6(RET):c.2758A>G (p.Ile920Val)	rs527787676	0.00001
NM_020975.6(RET):c.2776C>G (p.His926Asp)	rs774215008	0.00001
NM_020975.6(RET):c.2802-4G>T	rs878855061	0.00001
NM_020975.6(RET):c.3057G>A (p.Ala1019=)	rs369579749	0.00001
NM_020975.6(RET):c.884C>T (p.Thr295Met)	rs758159521	0.00001
NM_004304.5(ALK):c.3098T>A (p.Leu1033His)	rs572614173
NM_020975.6(RET):c.2030G>A (p.Arg677Gln)	rs536038262
NM_020975.6(RET):c.2111T>A (p.Val704Asp)
NM_020975.6(RET):c.2137-16del	rs1409965349
NM_020975.6(RET):c.2284+54C>A	rs566375223
NM_020975.6(RET):c.2348A>C (p.Asn783Thr)	rs587778656
NM_020975.6(RET):c.2393-14C>G	rs144269978
NM_020975.6(RET):c.2492G>T (p.Gly831Val)	rs760924186
NM_020975.6(RET):c.2523G>A (p.Pro841=)	rs56195026
NM_020975.6(RET):c.2531G>A (p.Arg844Gln)	rs55947360
NM_020975.6(RET):c.2554A>G (p.Ile852Val)	rs561276725
NM_020975.6(RET):c.2592T>C (p.Tyr864=)	rs1588877395
NM_020975.6(RET):c.2847A>G (p.Gly949=)	rs886046989
NM_020975.6(RET):c.3040-11C>G	rs1057517646
NM_020975.6(RET):c.44TGC[4] (p.Leu19del)	rs768132465

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