List of variants in gene INF2 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: 29

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HGVS	dbSNP	gnomAD frequency
NM_022489.4(INF2):c.105C>T (p.Pro35=)	rs4983530	0.98049
NM_022489.4(INF2):c.2640T>C (p.Asp880=)	rs10133301	0.88426
NM_022489.4(INF2):c.3066T>C (p.Asp1022=)	rs4983535	0.79980
NM_022489.4(INF2):c.2310+8del	rs3840006	0.58720
NM_022489.4(INF2):c.2775+15C>T	rs73347508	0.06749
NM_022489.4(INF2):c.3286C>T (p.Pro1096Ser)	rs34251364	0.05864
NM_022489.4(INF2):c.843+16C>T	rs118017785	0.05808
NM_022489.4(INF2):c.2322C>T (p.Thr774=)	rs59751492	0.02373
NM_022489.4(INF2):c.391+18A>T	rs115458897	0.02077
NM_022489.4(INF2):c.2571C>T (p.Ser857=)	rs62640005	0.01396
NM_022489.4(INF2):c.42G>A (p.Leu14=)	rs62638758	0.01192
NM_022489.4(INF2):c.3153C>T (p.Asp1051=)	rs117457867	0.01185
NM_022489.4(INF2):c.391+17G>A	rs4074531	0.01087
NM_022489.4(INF2):c.1281_1286del (p.Pro428_Leu429del)	rs751555478	0.00781
NM_022489.4(INF2):c.2630G>A (p.Arg877Gln)	rs142678449	0.00781
NM_022489.4(INF2):c.1547C>T (p.Pro516Leu)	rs111589086	0.00779
NM_022489.4(INF2):c.879G>A (p.Ser293=)	rs184709736	0.00543
NM_022489.4(INF2):c.3108T>C (p.Leu1036=)	rs186075307	0.00532
NM_022489.4(INF2):c.1078G>A (p.Val360Ile)	rs114820975	0.00483
NM_022489.4(INF2):c.3069C>T (p.Pro1023=)	rs75382114	0.00477
NM_022489.4(INF2):c.2458C>T (p.Arg820Trp)	rs79327775	0.00247
NM_022489.4(INF2):c.3404C>T (p.Thr1135Met)	rs3803311	0.00242
NM_022489.4(INF2):c.2138+9G>A	rs201065953	0.00213
NM_022489.4(INF2):c.2848C>T (p.Arg950Trp)	rs199873407	0.00098
NM_022489.4(INF2):c.3747G>A (p.Gln1249=)	rs149939482	0.00036
NM_022489.4(INF2):c.1506A>C (p.Pro502=)
NM_022489.4(INF2):c.3207A>C (p.Pro1069=)	rs1128840
NM_022489.4(INF2):c.3207A>G (p.Pro1069=)	rs1128840
NM_022489.4(INF2):c.391+6C>T	rs75115369

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