List of variants in gene SETD2 reported as benign for not specified

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_014159.7(SETD2):c.2704G>C (p.Glu902Gln)	rs58906143	0.01669
NM_014159.7(SETD2):c.3249A>C (p.Thr1083=)	rs80241480	0.00871
NM_014159.7(SETD2):c.2543C>T (p.Ala848Val)	rs75248784	0.00870
NM_014159.7(SETD2):c.2783C>G (p.Thr928Arg)	rs72895708	0.00228
NM_014159.7(SETD2):c.4320A>T (p.Pro1440=)	rs74485823	0.00191
NM_014159.7(SETD2):c.3567C>T (p.Thr1189=)	rs140803915	0.00131
NM_014159.7(SETD2):c.3097A>G (p.Thr1033Ala)	rs145759179	0.00063
NM_014159.7(SETD2):c.1885A>G (p.Lys629Glu)	rs145650484	0.00047
NM_014159.7(SETD2):c.2798G>T (p.Gly933Val)	rs202209141	0.00010
NM_014159.7(SETD2):c.2603A>G (p.Asp868Gly)	rs201752182	0.00003
NM_014159.7(SETD2):c.6686T>G (p.Val2229Gly)	rs377066147	0.00002

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