List of variants in gene WDR37 reported as uncertain significance for neurooculocardiogenitourinary syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_014023.4(WDR37):c.250G>A (p.Asp84Asn)	rs1255576929	0.00004
NM_014023.4(WDR37):c.808A>G (p.Ile270Val)	rs758141830	0.00001
NM_014023.4(WDR37):c.1444G>C (p.Gly482Arg)	rs1265219812
NM_014023.4(WDR37):c.344C>T (p.Thr115Ile)	rs1833994284
NM_014023.4(WDR37):c.770C>A (p.Pro257His)	rs1834896131
NM_014023.4(WDR37):c.808A>C (p.Ile270Leu)
NM_014023.4(WDR37):c.850G>T (p.Val284Phe)	rs2131662062
NM_014023.4(WDR37):c.928G>A (p.Val310Met)	rs1018536630

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