List of variants in gene combination LOC130003710, RET reported as likely benign for Multiple endocrine neoplasia, type 2

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.2801+9G>A	rs780912886	0.00001
NM_020975.6(RET):c.2799T>C (p.Asp933=)
NM_020975.6(RET):c.2801+11del	rs2132987306
NM_020975.6(RET):c.2801+12T>C
NM_020975.6(RET):c.2801+13G>A	rs2132987373
NM_020975.6(RET):c.2801+15T>C
NM_020975.6(RET):c.2801+17C>T	rs2132987446
NM_020975.6(RET):c.2801+19C>A
NM_020975.6(RET):c.2801+19C>G
NM_020975.6(RET):c.2801+19C>T
NM_020975.6(RET):c.2801+7G>A	rs1588878699
NM_020975.6(RET):c.2801+7G>T
NM_020975.6(RET):c.2801+8T>C	rs2132987232
NM_020975.6(RET):c.2801+8_2801+9del	rs1445588303

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