List of variants in gene SETD2 reported as likely 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_014159.7(SETD2):c.5316A>G (p.Glu1772=)	rs141027201	0.00014
NM_014159.7(SETD2):c.3890G>A (p.Arg1297His)	rs370953553	0.00004
NM_014159.7(SETD2):c.3168G>A (p.Ser1056=)	rs768944836	0.00003
NM_014159.7(SETD2):c.2431A>G (p.Asn811Asp)	rs1015887716	0.00001
NM_014159.7(SETD2):c.2997A>G (p.Val999=)	rs1387514420	0.00001
NM_014159.7(SETD2):c.4918-78AC[17]	rs61571386
NM_014159.7(SETD2):c.5268A>G (p.Glu1756=)	rs752039809
NM_014159.7(SETD2):c.6110-27_6110-26del	rs10589946
NM_014159.7(SETD2):c.6293+4dup	rs533328208
NM_014159.7(SETD2):c.6963+5C>G	rs1553683838

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