List of variants reported as likely benign for Multiple endocrine neoplasia type 2A by Myriad Genetics, Inc.

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Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 43

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.2372A>T (p.Tyr791Phe)	rs77724903	0.00178
NM_020975.6(RET):c.1946C>T (p.Ser649Leu)	rs148935214	0.00039
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.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.1880-13C>A	rs948277023	0.00009
NM_020975.6(RET):c.2657G>A (p.Arg886Gln)	rs373594744	0.00009
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.1942G>A (p.Val648Ile)	rs77711105	0.00007
NM_020975.6(RET):c.1597G>A (p.Gly533Ser)	rs75873440	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.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.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.2285-4T>G	rs376601566	0.00003
NM_020975.6(RET):c.2041C>G (p.Gln681Glu)	rs567241943	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.1915G>A (p.Ala639Thr)	rs777122776	0.00001
NM_020975.6(RET):c.1921G>A (p.Ala641Thr)	rs377767411	0.00001
NM_020975.6(RET):c.2365A>G (p.Lys789Glu)	rs1352006130	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.884C>T (p.Thr295Met)	rs758159521	0.00001
NM_020975.6(RET):c.2030G>A (p.Arg677Gln)	rs536038262
NM_020975.6(RET):c.2111T>A (p.Val704Asp)
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.2531G>A (p.Arg844Gln)	rs55947360
NM_020975.6(RET):c.2554A>G (p.Ile852Val)	rs561276725

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