List of variants in gene SUCLG2 reported as benign by PreventionGenetics, part of Exact Sciences

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_003848.4(SUCLG2):c.85-20C>T	rs2290174	0.49682
NM_001177599.2(SUCLG2):c.1210T>C (p.Tyr404His)	rs902321	0.40604
NM_001177599.2(SUCLG2):c.1273G>A (p.Val425Ile)	rs902320	0.24632
NM_003848.4(SUCLG2):c.1141C>T (p.Arg381Trp)	rs7623258	0.05819
NM_003848.4(SUCLG2):c.302A>G (p.Lys101Arg)	rs74675534	0.00500
NM_003848.4(SUCLG2):c.1184-7C>T
NM_003848.4(SUCLG2):c.1186A>G (p.Thr396Ala)
NM_003848.4(SUCLG2):c.758-10_758-8del	rs150352166

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