List of variants in gene combination LOC106736614, RET reported as likely benign for Multiple endocrine neoplasia, type 2

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.6G>A (p.Ala2=)	rs1243883489	0.00004
NM_020975.6(RET):c.31C>A (p.Leu11Met)	rs587780812	0.00003
NM_020975.6(RET):c.30G>A (p.Gly10=)	rs1050242868	0.00002
NM_020975.6(RET):c.15G>C (p.Thr5=)	rs1226499208	0.00001
NM_020975.6(RET):c.18C>T (p.Ser6=)	rs1185431356	0.00001
NM_020975.6(RET):c.15G>A (p.Thr5=)
NM_020975.6(RET):c.31C>T (p.Leu11=)	rs587780812
NM_020975.6(RET):c.6G>T (p.Ala2=)

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