ClinVar Miner

List of variants in gene combination LOC126862483, TP53, WRAP53 reported as uncertain significance for not specified

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.-111A>G	rs17884410	0.00012
NM_000546.6(TP53):c.-48G>A	rs531575965	0.00003

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