ClinVar Miner

List of variants in gene combination LOC126862483, TP53, WRAP53 studied for Hereditary cancer-predisposing syndrome

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.-29+269G>A	rs869312655	0.00017
NM_000546.6(TP53):c.-29+1G>C	rs2151082372
NM_000546.6(TP53):c.-29+1del	rs2151082385

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