List of variants in gene combination LOC110121502, MCS+9.7, RET reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.73+9390C>T	rs951233491	0.00001
NM_020975.6(RET):c.73+9405G>A	rs1165547757	0.00001
NM_020975.6(RET):c.73+9408A>G	rs963402218	0.00001
NM_020975.6(RET):c.73+9385_73+9395del	rs368137511
NM_020975.6(RET):c.73+9398G>A	rs749655572

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