List of variants in gene FGD4 reported as benign for not provided

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: 15

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HGVS	dbSNP
NM_001370298.3(FGD4):c.2173-322del	rs150852537
NM_139241.3(FGD4):c.1133-135G>A	rs10844252
NM_139241.3(FGD4):c.1133-236T>G	rs1004968
NM_139241.3(FGD4):c.1338+200A>C	rs10844254
NM_139241.3(FGD4):c.1515T>C (p.Ser505=)	rs60803891
NM_139241.3(FGD4):c.1636-292C>T	rs11052111
NM_139241.3(FGD4):c.1711C>A (p.Pro571Thr)	rs144693221
NM_139241.3(FGD4):c.1761+200G>A	rs1909510
NM_139241.3(FGD4):c.1762-257C>T	rs11831099
NM_139241.3(FGD4):c.2044-236G>A	rs10771973
NM_139241.3(FGD4):c.2044-46A>G	rs74073032
NM_139241.3(FGD4):c.836+10G>T	rs41276676
NM_139241.3(FGD4):c.837-149T>G	rs4931640
NM_139241.3(FGD4):c.837-37T>A	rs4931641
NM_139241.3(FGD4):c.993+149T>C	rs7964734

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