ClinVar Miner

List of variants in gene PIEZO2 reported as uncertain significance for autosomal recessive PIEZO2 associated disease

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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_001378183.1(PIEZO2):c.3730G>A (p.Val1244Met)	rs73946020	0.00561
NM_001378183.1(PIEZO2):c.4367G>A (p.Ser1456Asn)	rs1568013762	0.00001

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