ClinVar Miner

List of variants in gene combination LOC130062899, STK11 reported as uncertain significance for Familial ovarian cancer

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000455.5(STK11):c.1040C>T (p.Ala347Val)	rs587782058	0.00002
NM_000455.5(STK11):c.1108+11C>T	rs368857989	0.00001

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