List of variants in gene FRAS1 reported as likely pathogenic by CeGaT Center for Human Genetics Tuebingen

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_025074.7(FRAS1):c.3973C>T (p.Gln1325Ter)	rs1578291638
NM_025074.7(FRAS1):c.5125C>T (p.Arg1709Ter)	rs775517752
NM_025074.7(FRAS1):c.7522+2_7522+4del	rs1719735626

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