List of variants in gene RAF1 reported as benign for cardiovascular disorder

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: 30

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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.*348T>C	rs5746247	0.01554
NM_002880.4(RAF1):c.-281C>G	rs61761285	0.01090
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.*495C>T	rs12808	0.00354
NM_002880.4(RAF1):c.*190G>A	rs528863135	0.00335
NM_002880.4(RAF1):c.*160C>T	rs5746246	0.00295
NM_002880.4(RAF1):c.*110T>C	rs550188508	0.00112
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.321-14T>A	rs3730270	0.00032
NM_002880.4(RAF1):c.909A>C (p.Thr303=)	rs5746219	0.00025
NM_002880.4(RAF1):c.125C>T (p.Ala42Val)	rs11549992	0.00021
NM_002880.4(RAF1):c.119G>A (p.Arg40His)	rs192632236	0.00016
NM_002880.4(RAF1):c.122G>A (p.Arg41Gln)	rs145611571	0.00016
NM_002880.4(RAF1):c.*556G>A	rs187286358	0.00014
NM_002880.4(RAF1):c.680+6T>C	rs371846795	0.00014
NM_002880.4(RAF1):c.*404G>A	rs150460686	0.00013
NM_002880.4(RAF1):c.94A>G (p.Ile32Val)	rs372738063	0.00013
NM_002880.4(RAF1):c.1721A>G (p.Tyr574Cys)	rs370242565	0.00012
NM_002880.4(RAF1):c.1141G>A (p.Asp381Asn)	rs559632360	0.00001
NM_002880.4(RAF1):c.1914G>A (p.Thr638=)	rs144876026	0.00001
NM_002880.4(RAF1):c.*266C>T	rs1051208
NM_002880.4(RAF1):c.*606A>G	rs556460176
NM_002880.4(RAF1):c.*83C>T	rs2229757
NM_002880.4(RAF1):c.-267G>A	rs116247741
NM_002880.4(RAF1):c.1108+9_1108+21del	rs727504451
NM_002880.4(RAF1):c.1629G>C (p.Thr543=)	rs5746244
NM_002880.4(RAF1):c.1668+10_1668+11del	rs730880997

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