List of variants reported as likely benign by Medical Genetics, University of Parma

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Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_001042492.3(NF1):c.655-37A>C	rs375655707	0.00014
NM_001042492.3(NF1):c.3974+141T>C	rs779226804	0.00013
NM_001042492.3(NF1):c.4526G>A (p.Arg1509His)	rs546073780	0.00006
NM_001042492.3(NF1):c.3883A>G (p.Thr1295Ala)	rs143836226	0.00004
NM_001042492.3(NF1):c.584A>G (p.Lys195Arg)	rs587778552	0.00001
NM_001042492.3(NF1):c.7647A>G (p.Ser2549=)	rs750342324	0.00001
NM_001042492.3(NF1):c.1889T>A (p.Val630Glu)	rs1135402824
NM_001042492.3(NF1):c.2322T>C (p.Thr774=)	rs770111990
NM_001042492.3(NF1):c.4174-8_4174-6del	rs751729752
NM_001042492.3(NF1):c.7041T>C (p.Ser2347=)	rs746322836
NM_001042492.3(NF1):c.7416T>C (p.Pro2472=)	rs876659624
NM_001042492.3(NF1):c.7931C>A (p.Ala2644Glu)	rs766494934

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