Variants in gene FAT4 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_001291303.3(FAT4):c.2811G>T (p.Lys937Asn)	rs112454576	0.00367
NM_001291303.3(FAT4):c.3658T>A (p.Ser1220Thr)	rs181368820	0.00342
NM_001291303.3(FAT4):c.12070C>T (p.Arg4024Trp)	rs138019311	0.00333
NM_001291303.3(FAT4):c.3402A>T (p.Glu1134Asp)	rs144768563	0.00113
NM_001291303.3(FAT4):c.7052A>G (p.Asn2351Ser)	rs145105421	0.00096
NM_001291303.3(FAT4):c.11619C>T (p.Cys3873=)	rs141328606	0.00092
NM_001291303.3(FAT4):c.6985C>T (p.Arg2329Cys)	rs148293496	0.00009
NM_001291303.3(FAT4):c.3515C>T (p.Thr1172Ile)	rs535333070

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