ClinVar Miner

List of variants in gene combination LOC130004273, PTEN reported as uncertain significance for Macrocephaly-autism syndrome; Familial meningioma; Glioma susceptibility 2; Familial prostate cancer; Cowden syndrome 1

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)
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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000314.8(PTEN):c.-835C>T	rs587779994	0.00011
NM_000314.8(PTEN):c.-868G>A
NM_000314.8(PTEN):c.-904G>C	rs1044322

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