List of variants in gene FREM2 reported as benign by Eurofins NTD LLC (GA)

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_207361.6(FREM2):c.2233= (p.Pro745=)	rs2496423	0.99994
NM_207361.6(FREM2):c.3209T>C (p.Phe1070Ser)	rs2496425	0.43515
NM_207361.6(FREM2):c.1542C>T (p.Ala514=)	rs12874397	0.18215
NM_207361.6(FREM2):c.2250C>T (p.Asp750=)	rs41292755	0.07615
NM_207361.6(FREM2):c.303C>A (p.Pro101=)	rs8002488	0.05332
NM_207361.6(FREM2):c.5003G>A (p.Arg1668His)	rs1868463	0.05268
NM_207361.6(FREM2):c.8902G>A (p.Val2968Ile)	rs116099212	0.00379
NM_207361.6(FREM2):c.6925+7G>T	rs79530106	0.00364
NM_207361.6(FREM2):c.8460C>G (p.Ala2820=)	rs138775857	0.00325
NM_207361.6(FREM2):c.7335T>C (p.Gly2445=)	rs141921562	0.00276
NM_207361.6(FREM2):c.9071A>G (p.Asn3024Ser)	rs115149211	0.00261
NM_207361.6(FREM2):c.84C>G (p.Pro28=)	rs141718695	0.00194
NM_207361.6(FREM2):c.4686T>C (p.Asp1562=)	rs17058435	0.00172
NM_207361.6(FREM2):c.2133G>A (p.Met711Ile)	rs115446826	0.00052
NM_207361.6(FREM2):c.7520-5dup	rs36084034
NM_207361.6(FREM2):c.7520-6_7520-5dup	rs36084034

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