List of variants in gene combination LOC105371856, TANC2 reported as likely pathogenic by University of Washington Center for Mendelian Genomics, University of Washington

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_001394998.1(TANC2):c.3003del (p.Ala1002fs)	rs2047893330
NM_001394998.1(TANC2):c.3418C>T (p.Arg1140Ter)	rs2048464266
NM_001394998.1(TANC2):c.3765+1G>T	rs2048707664

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