List of variants in gene PLEKHA7 reported as uncertain significance by University of Washington Center for Mendelian Genomics, University of Washington

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
NM_001329630.2(PLEKHA7):c.53G>T (p.Gly18Val)	rs1865545338
NM_001329630.2(PLEKHA7):c.643G>A (p.Val215Met)	rs1028264032
NM_001329630.2(PLEKHA7):c.914A>T (p.Asn305Ile)	rs146091349

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