List of variants in gene TARDBP reported as likely 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_007375.4(TARDBP):c.*208G>A	rs148414479	0.02413
NM_007375.4(TARDBP):c.402+191C>T	rs72870034	0.01643
NM_007375.4(TARDBP):c.238+86A>G	rs55825417	0.01027
NM_007375.4(TARDBP):c.543+265A>G	rs74054480	0.00967
NM_007375.4(TARDBP):c.544-156A>G	rs146134526	0.00719
NM_007375.4(TARDBP):c.714+79C>T	rs138995559	0.00680
NM_007375.4(TARDBP):c.675A>G (p.Pro225=)	rs61741294	0.00675
NM_007375.4(TARDBP):c.714+277T>C	rs115612051	0.00566
NM_007375.4(TARDBP):c.544-184C>T	rs142943740	0.00395
NM_007375.4(TARDBP):c.543+290A>G	rs184723358	0.00358
NM_007375.4(TARDBP):c.239-116G>T	rs74054478
NM_007375.4(TARDBP):c.402+213dup	rs61443822
NM_007375.4(TARDBP):c.715-243C>T	rs146469040

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