List of variants in gene BPTF reported as benign by GeneDx

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_182641.4(BPTF):c.7927-6T>C	rs8068790	0.88251
NM_182641.4(BPTF):c.2271G>A (p.Leu757=)	rs7214985	0.03029
NM_182641.4(BPTF):c.36C>G (p.Pro12=)	rs868242186	0.02432
NM_182641.4(BPTF):c.8035GCCCCTCCA[3] (p.2676APP[4])	rs60308484
NM_182641.4(BPTF):c.8035GCCCCTCCA[5] (p.2676APP[6])	rs60308484

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