List of variants in gene POT1 reported as uncertain significance for hereditary epidermal appendage anomaly

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_015450.3(POT1):c.1294C>T (p.Arg432Ter)	rs758341603
NM_015450.3(POT1):c.437C>T (p.Pro146Leu)	rs1554426915
NM_015450.3(POT1):c.728G>A (p.Ser243Asn)

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