Variants in gene RAF1 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 8

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HGVS	dbSNP	gnomAD frequency
NM_002880.4(RAF1):c.212A>G (p.Asn71Ser)	rs184022679	0.00029
NM_002880.4(RAF1):c.122G>A (p.Arg41Gln)	rs145611571	0.00016
NM_002880.4(RAF1):c.680+6T>C	rs371846795	0.00014
NM_002880.4(RAF1):c.1721A>G (p.Tyr574Cys)	rs370242565	0.00012
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.124_125delinsAT (p.Ala42Ile)	rs876657965
NM_002880.4(RAF1):c.1629G>C (p.Thr543=)	rs5746244

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