List of variants in gene FIG4 reported as likely 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: 25

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HGVS	dbSNP	gnomAD frequency
NM_014845.6(FIG4):c.447-16G>T	rs200890189	0.00618
NM_014845.6(FIG4):c.1584-8T>A	rs199522051	0.00086
NM_014845.6(FIG4):c.834A>T (p.Lys278Asn)	rs138048706	0.00029
NM_014845.6(FIG4):c.1271+5A>G	rs374583399	0.00012
NM_014845.6(FIG4):c.2459+7T>G	rs575271308	0.00009
NM_014845.6(FIG4):c.717A>G (p.Lys239=)	rs750904354	0.00009
NM_014845.6(FIG4):c.658A>G (p.Ile220Val)	rs565096937	0.00006
NM_014845.6(FIG4):c.1435-8C>T	rs754607430	0.00005
NM_014845.6(FIG4):c.584A>T (p.Gln195Leu)	rs749696803	0.00005
NM_014845.6(FIG4):c.33G>C (p.Ser11=)	rs527523781	0.00004
NM_014845.6(FIG4):c.2232C>T (p.Ser744=)	rs760578430	0.00003
NM_014845.6(FIG4):c.351G>A (p.Ala117=)	rs375963892	0.00003
NM_014845.6(FIG4):c.497+9G>A	rs759409330	0.00002
NM_014845.6(FIG4):c.1525C>T (p.Leu509=)	rs146488614	0.00001
NM_014845.6(FIG4):c.1827G>A (p.Glu609=)	rs756085095	0.00001
NM_014845.6(FIG4):c.2403A>G (p.Leu801=)	rs1048137431	0.00001
NM_014845.6(FIG4):c.166-5C>T
NM_014845.6(FIG4):c.1833A>G (p.Pro611=)
NM_014845.6(FIG4):c.2097-10C>G	rs142482745
NM_014845.6(FIG4):c.2377-11_2377-10del	rs200535694
NM_014845.6(FIG4):c.2547-3T>C
NM_014845.6(FIG4):c.2568G>T (p.Ser856=)	rs140055056
NM_014845.6(FIG4):c.401A>C (p.Tyr134Ser)	rs571563767
NM_014845.6(FIG4):c.497+7G>A	rs140111950
NM_014845.6(FIG4):c.640G>A (p.Gly214Arg)	rs529048339

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