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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001291303.3(FAT4):c.12091G>A (p.Glu4031Lys)	rs1085307886
NM_001291303.3(FAT4):c.13627A>T (p.Lys4543Ter)	rs1553931042
NM_001291303.3(FAT4):c.2527C>T (p.Gln843Ter)	rs1064793943
NM_001291303.3(FAT4):c.6249dup (p.Tyr2084fs)
NM_001291303.3(FAT4):c.6843+1G>T	rs2126028189
NM_001291303.3(FAT4):c.7018+2T>C	rs2530788030

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