List of variants in gene FAT4 reported as likely pathogenic for not provided

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: 3

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HGVS	dbSNP
NM_024582.4(FAT4):c.12085G>A (p.Glu4029Lys)	rs1085307886
NM_024582.4(FAT4):c.13621A>T (p.Lys4541Ter)	rs1553931042
NM_024582.4(FAT4):c.2527C>T (p.Gln843Ter)	rs1064793943

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