List of variants in gene INF2 reported as likely benign for not provided

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: 101

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HGVS	dbSNP	gnomAD frequency
NM_022489.4(INF2):c.3478G>A (p.Gly1160Ser)	rs9672065	0.01930
NM_022489.4(INF2):c.843+294C>T	rs147294109	0.01772
NM_022489.4(INF2):c.668-82C>G	rs75836310	0.01467
NM_022489.4(INF2):c.2490-301G>A	rs112480223	0.01324
NM_022489.4(INF2):c.844-252T>C	rs112186582	0.01190
NM_022489.4(INF2):c.843+33C>T	rs145596224	0.01186
NM_022489.4(INF2):c.2489+115G>A	rs117278745	0.01184
NM_022489.4(INF2):c.701+281C>G	rs118092663	0.01180
NM_022489.4(INF2):c.1735+73G>A	rs146732870	0.01017
NM_022489.4(INF2):c.392-230C>T	rs74091142	0.00975
NM_022489.4(INF2):c.392-247C>G	rs115994445	0.00974
NM_022489.4(INF2):c.701+27C>T	rs55981430	0.00973
NM_022489.4(INF2):c.1888-33C>T	rs111887340	0.00949
NM_022489.4(INF2):c.843+212C>T	rs115533334	0.00857
NM_022489.4(INF2):c.3040+142G>A	rs115119366	0.00820
NM_022489.4(INF2):c.2878+23G>A	rs144778200	0.00698
NM_022489.4(INF2):c.1950-151A>G	rs149470784	0.00697
NM_022489.4(INF2):c.844-146T>C	rs117710656	0.00612
NM_022489.4(INF2):c.2239+165C>T	rs562266294	0.00582
NM_022489.4(INF2):c.1263A>C (p.Pro421=)	rs761903419	0.00483
NM_022489.4(INF2):c.1451G>A (p.Cys484Tyr)	rs201323100	0.00470
NM_022489.4(INF2):c.*1+142C>T	rs142139206	0.00466
NM_022489.4(INF2):c.-9-302C>G	rs76259288	0.00465
NM_022489.4(INF2):c.2775+97G>A	rs146906579	0.00330
NM_022489.4(INF2):c.2489+200G>A	rs148878017	0.00327
NM_022489.4(INF2):c.*388A>G	rs140513391	0.00296
NM_022489.4(INF2):c.*544G>A	rs111978619	0.00287
NM_022489.4(INF2):c.2458C>T (p.Arg820Trp)	rs79327775	0.00247
NM_022489.4(INF2):c.558C>T (p.Ser186=)	rs150714865	0.00158
NM_022489.4(INF2):c.3244G>T (p.Ala1082Ser)	rs143540449	0.00150
NM_022489.4(INF2):c.3134G>A (p.Arg1045Gln)	rs200369827	0.00126
NM_022489.4(INF2):c.2848C>T (p.Arg950Trp)	rs199873407	0.00098
NM_022489.4(INF2):c.507+7G>A	rs201568246	0.00095
NM_022489.4(INF2):c.1950-10C>T	rs199987321	0.00082
NM_022489.4(INF2):c.2489+21C>T	rs201432578	0.00076
NM_022489.4(INF2):c.2611-42G>A	rs140767529	0.00068
NM_022489.4(INF2):c.2052+50G>A	rs201873894	0.00063
NM_022489.4(INF2):c.*16C>T	rs199912466	0.00058
NM_022489.4(INF2):c.1144A>G (p.Ser382Gly)	rs201077878	0.00048
NM_022489.4(INF2):c.3638G>A (p.Arg1213Gln)	rs199801767	0.00047
NM_022489.4(INF2):c.1966G>A (p.Ala656Thr)	rs189559257	0.00043
NM_022489.4(INF2):c.2181G>A (p.Ala727=)	rs370830904	0.00038
NM_022489.4(INF2):c.3221G>A (p.Arg1074Lys)	rs201445955	0.00036
NM_022489.4(INF2):c.37G>A (p.Ala13Thr)	rs201383094	0.00034
NM_022489.4(INF2):c.609C>T (p.Ala203=)	rs140017506	0.00028
NM_022489.4(INF2):c.3563C>T (p.Ser1188Phe)	rs201715539	0.00022
NM_022489.4(INF2):c.3103G>A (p.Gly1035Ser)	rs368995122	0.00019
NM_022489.4(INF2):c.2053A>G (p.Ile685Val)	rs199526439	0.00016
NM_022489.4(INF2):c.1736-6C>T	rs371991103	0.00015
NM_022489.4(INF2):c.1360C>T (p.Leu454Phe)	rs545495465	0.00012
NM_022489.4(INF2):c.744C>T (p.Phe248=)	rs372799744	0.00012
NM_022489.4(INF2):c.1770C>T (p.Pro590=)	rs549506051	0.00011
NM_022489.4(INF2):c.844-6G>A	rs370399987	0.00011
NM_022489.4(INF2):c.1409C>A (p.Ala470Asp)	rs1166010216	0.00010
NM_022489.4(INF2):c.67T>A (p.Ser23Thr)	rs746964937	0.00010
NM_022489.4(INF2):c.1197C>T (p.His399=)	rs746493706	0.00009
NM_022489.4(INF2):c.3654C>T (p.Thr1218=)	rs557462297	0.00009
NM_022489.4(INF2):c.3695-21G>A	rs200543313	0.00009
NM_022489.4(INF2):c.798C>G (p.Val266=)	rs375005967	0.00009
NM_022489.4(INF2):c.3157G>A (p.Val1053Met)	rs760721935	0.00008
NM_022489.4(INF2):c.668-12G>A	rs367924307	0.00008
NM_022489.4(INF2):c.*1+1G>C	rs758452999	0.00007
NM_022489.4(INF2):c.1304C>T (p.Ala435Val)	rs777455096	0.00007
NM_022489.4(INF2):c.1377G>A (p.Pro459=)	rs776870726	0.00007
NM_022489.4(INF2):c.3082C>T (p.Arg1028Cys)	rs369987125	0.00007
NM_022489.4(INF2):c.597C>T (p.Ser199=)	rs372269719	0.00007
NM_022489.4(INF2):c.1448C>T (p.Ser483Phe)	rs753188664	0.00006
NM_022489.4(INF2):c.2459G>A (p.Arg820Gln)	rs759989953	0.00006
NM_022489.4(INF2):c.885G>A (p.Leu295=)	rs370680236	0.00006
NM_022489.4(INF2):c.3631C>T (p.Arg1211Trp)	rs374049468	0.00005
NM_022489.4(INF2):c.2043G>A (p.Glu681=)	rs776591878	0.00004
NM_022489.4(INF2):c.2084G>A (p.Arg695Gln)	rs372333024	0.00004
NM_022489.4(INF2):c.3461A>T (p.Asp1154Val)	rs753263522	0.00004
NM_022489.4(INF2):c.510G>A (p.Thr170=)	rs750711173	0.00004
NM_022489.4(INF2):c.519C>T (p.Ser173=)	rs780247558	0.00004
NM_022489.4(INF2):c.2310C>T (p.Tyr770=)	rs758454108	0.00003
NM_022489.4(INF2):c.2311-4C>G	rs371953149	0.00003
NM_022489.4(INF2):c.2418+19G>A	rs770701500	0.00003
NM_022489.4(INF2):c.1615G>A (p.Val539Met)	rs769014945	0.00002
NM_022489.4(INF2):c.1965C>T (p.Val655=)	rs752090814	0.00002
NM_022489.4(INF2):c.1115C>T (p.Ser372Phe)	rs770882784	0.00001
NM_022489.4(INF2):c.2188G>A (p.Val730Met)	rs373199310	0.00001
NM_022489.4(INF2):c.2550C>T (p.Thr850=)	rs771112980	0.00001
NM_022489.4(INF2):c.2769C>T (p.Ala923=)	rs370426339	0.00001
NM_022489.4(INF2):c.654G>T (p.Arg218=)	rs745354738	0.00001
NM_022489.4(INF2):c.-9-240G>T	rs556761581
NM_022489.4(INF2):c.1377G>C (p.Pro459=)	rs776870726
NM_022489.4(INF2):c.1500G>C (p.Pro500=)	rs755670925
NM_022489.4(INF2):c.1582C>T (p.Pro528Ser)	rs181694819
NM_022489.4(INF2):c.1716G>C (p.Leu572=)	rs780141010
NM_022489.4(INF2):c.2388C>T (p.Asn796=)
NM_022489.4(INF2):c.2397G>A (p.Thr799=)
NM_022489.4(INF2):c.2418+47C>T	rs751037480
NM_022489.4(INF2):c.2611-41C>A	rs145794141
NM_022489.4(INF2):c.2750G>A (p.Arg917Gln)
NM_022489.4(INF2):c.2751G>A (p.Arg917=)
NM_022489.4(INF2):c.2776-81C>G	rs138919548
NM_022489.4(INF2):c.2878+22G>C	rs201633273
NM_022489.4(INF2):c.2878+22G>T	rs201633273
NM_022489.4(INF2):c.3041-90G>A	rs146081430
NM_022489.4(INF2):c.985+65G>C	rs7147340

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