List of variants in gene FRAS1 reported as likely benign by Genetic Services Laboratory, University of Chicago

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_025074.7(FRAS1):c.9806G>A (p.Arg3269Gln)	rs61729366	0.00571
NM_025074.7(FRAS1):c.10539A>G (p.Thr3513=)	rs199921300	0.00088
NM_025074.7(FRAS1):c.6939C>T (p.Pro2313=)	rs150936204	0.00070
NM_025074.7(FRAS1):c.11871G>A (p.Arg3957=)	rs367585112	0.00019
NM_025074.7(FRAS1):c.11695C>T (p.Leu3899=)	rs367723684	0.00015
NM_025074.7(FRAS1):c.1535-4G>A	rs749569960	0.00005
NM_025074.7(FRAS1):c.4807C>T (p.Arg1603Trp)	rs961911715	0.00005
NM_025074.7(FRAS1):c.2046G>A (p.Val682=)	rs764188507

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