List of variants in gene FRAS1 reported as uncertain significance 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_025074.7(FRAS1):c.4579C>T (p.Arg1527Trp)	rs1872267	0.00253
NM_025074.7(FRAS1):c.2861C>T (p.Thr954Met)	rs17003166	0.00252
NM_025074.7(FRAS1):c.4095C>T (p.Ile1365=)	rs79869130	0.00088
NM_025074.7(FRAS1):c.9446C>T (p.Thr3149Met)	rs150680111	0.00080
NM_025074.7(FRAS1):c.9296G>A (p.Arg3099Gln)	rs149692526	0.00071
NM_025074.7(FRAS1):c.1607A>G (p.His536Arg)	rs193245098	0.00048
NM_025074.7(FRAS1):c.9356A>G (p.Asn3119Ser)	rs191105001	0.00016
NM_025074.7(FRAS1):c.3059G>A (p.Arg1020His)	rs773906563	0.00005
NM_025074.7(FRAS1):c.1687C>G (p.Gln563Glu)	rs1254192090	0.00001
NM_025074.7(FRAS1):c.4098C>T (p.Ile1366=)	rs1027609786	0.00001
NM_025074.7(FRAS1):c.1882C>A (p.Pro628Thr)	rs199542867

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