List of variants in gene FLT1 reported as likely benign by Breakthrough Genomics, Breakthrough Genomics

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_002019.4(FLT1):c.3602C>T (p.Pro1201Leu)	rs140861115	0.00303
NM_002019.4(FLT1):c.3552C>T (p.Tyr1184=)	rs55673217	0.00196
NM_002019.4(FLT1):c.1644A>G (p.Ile548Met)	rs148479824	0.00148
NM_002019.4(FLT1):c.321C>T (p.Cys107=)	rs142924808	0.00049

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