List of variants in gene combination LOC126862696, PIEZO2 reported as uncertain significance

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001378183.1(PIEZO2):c.2886T>G (p.Ile962Met)	rs1297735094	0.00001
NM_001378183.1(PIEZO2):c.2911G>A (p.Val971Ile)	rs1013027921	0.00001
NM_001378183.1(PIEZO2):c.2938G>T (p.Val980Leu)	rs1169323245

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