List of variants in gene GDF6 reported as likely benign by Illumina Laboratory Services, Illumina

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001001557.4(GDF6):c.1429_1430del	rs139734303	0.03848
NM_001001557.4(GDF6):c.852C>G (p.Ser284=)	rs74498875	0.00603
NM_001001557.4(GDF6):c.255G>T (p.Pro85=)	rs112296824	0.00366
NM_001001557.4(GDF6):c.746C>A (p.Ala249Glu)	rs121909352	0.00200
NM_001001557.4(GDF6):c.356A>G (p.Gln119Arg)	rs140579014	0.00061
NM_001001557.4(GDF6):c.250G>A (p.Glu84Lys)	rs148321868	0.00022
NM_001001557.3(GDF6):c.*2243G>C	rs142786788	0.00017
NM_001001557.4(GDF6):c.1304C>T (p.Ala435Val)	rs140782427	0.00014
NM_001001557.4(GDF6):c.1251C>T (p.Pro417=)	rs552124580	0.00006
NM_001001557.4(GDF6):c.1271A>G (p.Lys424Arg)	rs121909353	0.00003
NM_001001557.4(GDF6):c.1233C>T (p.Asp411=)	rs774375234	0.00002
NM_001001557.4(GDF6):c.407-5C>T	rs758091453	0.00001
NM_001001557.4(GDF6):c.817C>A (p.Gln273Lys)	rs780167779	0.00001
NM_001001557.4(GDF6):c.955G>A (p.Ala319Thr)	rs779322747

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