List of variants in gene FREM2 reported as uncertain significance 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: 42

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HGVS	dbSNP	gnomAD frequency
NM_207361.6(FREM2):c.9113T>C (p.Val3038Ala)	rs114688149	0.00204
NM_207361.6(FREM2):c.5642-9T>C	rs148794835	0.00141
NM_207361.6(FREM2):c.2740T>G (p.Cys914Gly)	rs146685625	0.00127
NM_207361.6(FREM2):c.9038C>T (p.Thr3013Met)	rs114400765	0.00118
NM_207361.6(FREM2):c.2367G>A (p.Pro789=)	rs140101984	0.00095
NM_207361.6(FREM2):c.1580C>T (p.Ser527Leu)	rs139804851	0.00084
NM_207361.6(FREM2):c.177T>C (p.Gly59=)	rs370018440	0.00079
NM_207361.6(FREM2):c.2823C>T (p.Pro941=)	rs150154438	0.00079
NM_207361.6(FREM2):c.8918A>G (p.Lys2973Arg)	rs147506207	0.00047
NM_207361.6(FREM2):c.2754C>T (p.Val918=)	rs140353326	0.00046
NM_207361.6(FREM2):c.181G>C (p.Ala61Pro)	rs553605556	0.00032
NM_207361.6(FREM2):c.6860T>C (p.Ile2287Thr)	rs200983871	0.00029
NM_207361.6(FREM2):c.7062G>A (p.Thr2354=)	rs41286130	0.00026
NM_207361.6(FREM2):c.9009C>T (p.Val3003=)	rs145657148	0.00026
NM_207361.6(FREM2):c.8906T>C (p.Leu2969Pro)	rs140937193	0.00019
NM_207361.6(FREM2):c.4567C>T (p.Arg1523Cys)	rs200817424	0.00018
NM_207361.6(FREM2):c.2801G>A (p.Arg934Gln)	rs145484598	0.00013
NM_207361.6(FREM2):c.6421G>A (p.Glu2141Lys)	rs376602370	0.00013
NM_207361.6(FREM2):c.6743-9C>T	rs749834830	0.00013
NM_207361.6(FREM2):c.1737C>T (p.Ile579=)	rs144811771	0.00012
NM_207361.6(FREM2):c.6333C>T (p.Gly2111=)	rs116763572	0.00010
NM_207361.6(FREM2):c.3785G>C (p.Ser1262Thr)	rs753652530	0.00006
NM_207361.6(FREM2):c.6272C>T (p.Ala2091Val)	rs374178459	0.00006
NM_207361.6(FREM2):c.6807G>A (p.Ser2269=)	rs752080876	0.00005
NM_207361.6(FREM2):c.38G>A (p.Arg13Gln)	rs765718616	0.00004
NM_207361.6(FREM2):c.5276T>C (p.Leu1759Ser)	rs750450348	0.00004
NM_207361.6(FREM2):c.6004C>T (p.Pro2002Ser)	rs372782469	0.00004
NM_207361.6(FREM2):c.4283G>A (p.Gly1428Glu)	rs369891021	0.00003
NM_207361.6(FREM2):c.6016G>C (p.Asp2006His)	rs1231644914	0.00003
NM_207361.6(FREM2):c.6499C>T (p.Arg2167Trp)	rs114837786	0.00003
NM_207361.6(FREM2):c.7177G>A (p.Ala2393Thr)	rs769767420	0.00001
NM_207361.6(FREM2):c.4321A>G (p.Thr1441Ala)	rs886042127
NM_207361.6(FREM2):c.4331T>C (p.Leu1444Pro)	rs886042126
NM_207361.6(FREM2):c.4588G>C (p.Asp1530His)	rs886043214
NM_207361.6(FREM2):c.5059_5060inv (p.Glu1687Ser)
NM_207361.6(FREM2):c.5120G>A (p.Gly1707Glu)	rs886044224
NM_207361.6(FREM2):c.5858A>G (p.Asp1953Gly)	rs794727814
NM_207361.6(FREM2):c.6177A>G (p.Thr2059=)	rs794727940
NM_207361.6(FREM2):c.6490T>C (p.Cys2164Arg)	rs886042926
NM_207361.6(FREM2):c.7329T>A (p.Pro2443=)	rs1303270704
NM_207361.6(FREM2):c.7520-10_7520-9insCT	rs1399473815
NM_207361.6(FREM2):c.8206G>A (p.Gly2736Ser)	rs368732492

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