List of variants in gene SETD2 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: 32

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HGVS	dbSNP	gnomAD frequency
NM_014159.7(SETD2):c.7238+269G>C	rs79545841	0.03068
NM_014159.7(SETD2):c.7098+320C>T	rs138535378	0.03035
NM_014159.7(SETD2):c.72-66A>G	rs11717033	0.03026
NM_014159.7(SETD2):c.6110-302A>G	rs151302053	0.01455
NM_014159.7(SETD2):c.4872T>A (p.Ser1624=)	rs75763513	0.01071
NM_014159.7(SETD2):c.5278-257A>T	rs6771992	0.00956
NM_014159.7(SETD2):c.5143-47T>G	rs183862100	0.00954
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.72-152dup	rs200216979	0.00789
NM_014159.7(SETD2):c.557C>T (p.Pro186Leu)	rs78759480	0.00723
NM_014159.7(SETD2):c.7432-102A>T	rs150163751	0.00675
NM_014159.7(SETD2):c.6060+266C>T	rs181463154	0.00644
NM_014159.7(SETD2):c.4586+123A>T	rs183601200	0.00635
NM_014159.7(SETD2):c.7238+53G>A	rs139159960	0.00560
NM_014159.7(SETD2):c.4918-76A>G	rs932394374	0.00379
NM_014159.7(SETD2):c.5277+117A>G	rs138282303	0.00369
NM_014159.7(SETD2):c.5143-240T>G	rs529665591	0.00343
NM_014159.7(SETD2):c.7098+235C>T	rs144641521	0.00305
NM_014159.7(SETD2):c.5143-20A>G	rs201987175	0.00123
NM_014159.7(SETD2):c.4320A>T (p.Pro1440=)	rs74485823	0.00080
NM_014159.7(SETD2):c.265C>T (p.Leu89Phe)	rs374799616	0.00015
NM_014159.7(SETD2):c.2024G>A (p.Gly675Glu)	rs568134733	0.00002
NM_014159.7(SETD2):c.6686T>G (p.Val2229Gly)	rs377066147	0.00002
NM_014159.7(SETD2):c.4839+72dup	rs55987628
NM_014159.7(SETD2):c.4918-78AC[20]	rs61571386
NM_014159.7(SETD2):c.5397+335_5397+336del	rs140225710
NM_014159.7(SETD2):c.5398-60dup	rs5848822
NM_014159.7(SETD2):c.6061-314_6061-313dup	rs548953692
NM_014159.7(SETD2):c.6110-39dup	rs10589946
NM_014159.7(SETD2):c.6293+4dup	rs533328208
NM_014159.7(SETD2):c.6963+5C>G	rs1553683838

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