List of variants in gene combination LOC106736614, RET reported as likely benign for adrenal gland neoplasm

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_020975.5(RET):c.-196C>A	rs10900297	0.41632
NM_020975.6(RET):c.31C>T (p.Leu11=)	rs587780812

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