List of variants in gene FRAS1 reported as likely benign by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_025074.7(FRAS1):c.3151+14_3151+15dup	rs398092530	0.38519
NM_025074.7(FRAS1):c.9806G>A (p.Arg3269Gln)	rs61729366	0.00592
NM_025074.7(FRAS1):c.5374G>A (p.Ala1792Thr)	rs150916370	0.00193
NM_025074.7(FRAS1):c.1918C>T (p.Arg640Cys)	rs147869493	0.00074
NM_025074.7(FRAS1):c.4334C>T (p.Thr1445Ile)	rs200123789	0.00034

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