List of variants in gene combination LOC111162620, TP63 reported as uncertain significance for orofacial cleft

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_003722.5(TP63):c.-65C>T	rs886058220	0.00001
NM_003722.5(TP63):c.-38T>C	rs1729451583
NM_003722.5(TP63):c.-3G>C	rs770510830
NM_003722.5(TP63):c.-87C>T	rs747090025

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