List of variants in gene FAT4 reported as likely benign by Clinical Genetics, Academic Medical Center

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.13554G>A (p.Leu4518=)	rs78235204	0.00273
NM_001291303.3(FAT4):c.10390A>G (p.Ile3464Val)	rs147872710	0.00237
NM_001291303.3(FAT4):c.5883T>C (p.Ser1961=)	rs117016099	0.00052
NM_001291303.3(FAT4):c.13206C>A (p.Gly4402=)	rs200101519	0.00032
NM_001291303.3(FAT4):c.12321T>C (p.Asn4107=)	rs200344963	0.00024
NM_001291303.3(FAT4):c.739C>A (p.Pro247Thr)	rs191329848

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