List of variants reported as likely benign for thyroid gland disorder by Color Diagnostics, LLC DBA Color Health

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

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.166C>A (p.Leu56Met)	rs145633958	0.00310
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.1017G>A (p.Ser339=)	rs369810881	0.00014
NM_020975.6(RET):c.597C>T (p.Asn199=)	rs55810667	0.00012
NM_020975.6(RET):c.3243T>C (p.Asp1081=)	rs144192900	0.00010
NM_020975.6(RET):c.1064-6C>T	rs768878280	0.00004
NM_020975.6(RET):c.1118C>T (p.Ala373Val)	rs546866208	0.00004
NM_020975.6(RET):c.2427C>T (p.Tyr809=)	rs577929869	0.00004
NM_020975.6(RET):c.693C>T (p.Arg231=)	rs576806329	0.00004
NM_020975.6(RET):c.1941C>T (p.Ile647=)	rs75225191	0.00002
NM_020975.6(RET):c.2358T>C (p.His786=)	rs758715544	0.00002
NM_020975.6(RET):c.30G>A (p.Gly10=)	rs1050242868	0.00002
NM_020975.6(RET):c.2784C>T (p.Tyr928=)	rs779594537	0.00001
NM_020975.6(RET):c.621G>A (p.Leu207=)	rs1343290853
NM_020975.6(RET):c.624G>T (p.Glu208Asp)	rs781750106

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