List of variants in gene RAF1 reported as benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 24

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HGVS	dbSNP	gnomAD frequency
NM_002880.4(RAF1):c.1669-13T>C	rs147475396	0.00819
NM_002880.4(RAF1):c.208-17T>C	rs3730268	0.00529
NM_002880.4(RAF1):c.321-14T>A	rs3730270	0.00032
NM_002880.4(RAF1):c.212A>G (p.Asn71Ser)	rs184022679	0.00029
NM_002880.4(RAF1):c.909A>C (p.Thr303=)	rs5746219	0.00025
NM_002880.4(RAF1):c.1537-11G>A	rs182394722	0.00024
NM_002880.4(RAF1):c.576A>G (p.Gln192=)	rs148759910	0.00016
NM_002880.4(RAF1):c.1587G>A (p.Ser529=)	rs114687276	0.00014
NM_002880.4(RAF1):c.680+6T>C	rs371846795	0.00014
NM_002880.4(RAF1):c.1107C>T (p.His369=)	rs761947194	0.00006
NM_002880.4(RAF1):c.1371-15C>A	rs371491379	0.00006
NM_002880.4(RAF1):c.570C>T (p.Ile190=)	rs780912024	0.00004
NM_002880.4(RAF1):c.1668+4A>G	rs771344560	0.00002
NM_002880.4(RAF1):c.639T>C (p.Thr213=)	rs397516823	0.00002
NM_002880.4(RAF1):c.1141G>A (p.Asp381Asn)	rs559632360	0.00001
NM_002880.4(RAF1):c.1193+18G>C	rs201845942	0.00001
NM_002880.4(RAF1):c.1914G>A (p.Thr638=)	rs144876026	0.00001
NM_002880.4(RAF1):c.907A>G (p.Thr303Ala)	rs775898894	0.00001
NM_002880.4(RAF1):c.1108+9_1108+21del	rs727504451
NM_002880.4(RAF1):c.124_125delinsAT (p.Ala42Ile)	rs876657965
NM_002880.4(RAF1):c.1629G>C (p.Thr543=)	rs5746244
NM_002880.4(RAF1):c.1668+10_1668+11del	rs730880997
NM_002880.4(RAF1):c.1668+19G>T	rs5746245
NM_002880.4(RAF1):c.321-14dup	rs202103447

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