List of variants in gene FREM1 reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_001379081.2(FREM1):c.3472-20T>C	rs77508679	0.01216
NM_001379081.2(FREM1):c.2337+19A>G	rs201898982	0.00158
NM_001379081.2(FREM1):c.5049C>T (p.Asn1683=)	rs200063334	0.00089
NM_001379081.2(FREM1):c.4867T>C (p.Leu1623=)	rs369101934	0.00064
NM_001379081.2(FREM1):c.4995C>T (p.Asp1665=)	rs372941168	0.00049
NM_001379081.2(FREM1):c.6279A>G (p.Val2093=)	rs373107801	0.00033
NM_001379081.2(FREM1):c.4941C>T (p.Tyr1647=)	rs373880888	0.00020
NM_001379081.2(FREM1):c.4983T>A (p.Pro1661=)	rs111333359	0.00006
NM_001379081.2(FREM1):c.3378A>G (p.Thr1126=)	rs202213402	0.00004
NM_001379081.2(FREM1):c.246C>T (p.Cys82=)	rs766485109	0.00003
NM_001379081.2(FREM1):c.3517G>T (p.Ala1173Ser)	rs564039071
NM_001379081.2(FREM1):c.4563C>A (p.Ala1521=)	rs60091943
NM_001379081.2(FREM1):c.483C>T (p.Phe161=)	rs540878376
NM_001379081.2(FREM1):c.516C>T (p.Thr172=)	rs41265310
NM_001379081.2(FREM1):c.5316G>T (p.Ser1772=)	rs775863172
NM_001379081.2(FREM1):c.5335-11del	rs140882884

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