List of variants in gene RAF1 reported as benign by Invitae

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_002880.4(RAF1):c.1755A>G (p.Val585=)	rs3730296	0.02125
NM_002880.4(RAF1):c.1669-13T>C	rs147475396	0.00819
NM_002880.4(RAF1):c.923C>T (p.Pro308Leu)	rs5746220	0.00571
NM_002880.4(RAF1):c.208-17T>C	rs3730268	0.00529
NM_002880.4(RAF1):c.1830A>G (p.Gln610=)	rs141791080	0.00088
NM_002880.4(RAF1):c.581+4A>G	rs201776526	0.00087
NM_002880.4(RAF1):c.320+19A>G	rs5746197	0.00061
NM_002880.4(RAF1):c.321-14T>A	rs3730270	0.00032
NM_002880.4(RAF1):c.1537-11G>A	rs182394722	0.00024
NM_002880.4(RAF1):c.119G>A (p.Arg40His)	rs192632236	0.00016
NM_002880.4(RAF1):c.1587G>A (p.Ser529=)	rs114687276	0.00014
NM_002880.4(RAF1):c.94A>G (p.Ile32Val)	rs372738063	0.00013
NM_002880.4(RAF1):c.1914G>A (p.Thr638=)	rs144876026	0.00001
NM_002880.4(RAF1):c.1629G>A (p.Thr543=)	rs5746244
NM_002880.4(RAF1):c.1668+19G>T	rs5746245
NM_002880.4(RAF1):c.321-14dup	rs202103447
NM_002880.4(RAF1):c.680+10dup

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