List of variants in gene combination MIR1225, PKD1, TSC2 reported as likely pathogenic

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: 3

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HGVS	dbSNP	gnomAD frequency
GRCh38/hg38 16p13.3(chr16:2089462-2092132)x1
NM_001009944.3(PKD1):c.11249G>A (p.Arg3750Gln)	rs1327414405
NM_001009944.3(PKD1):c.11412-2A>G

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