List of variants in gene combination LOC130003710, RET reported as uncertain significance for endocrine gland neoplasm

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.2801+9G>A	rs780912886	0.00001
NM_020975.5(RET):c.2731-?_*(1_?)del
NM_020975.6(RET):c.2791C>A (p.Gln931Lys)
NM_020975.6(RET):c.2801+3A>G	rs768284486

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