List of variants in gene ZNF408 reported as uncertain significance for cardiovascular disorder

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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_024741.3(ZNF408):c.457C>T (p.Leu153Phe)	rs140201502	0.00043
NM_024741.3(ZNF408):c.1928C>T (p.Ala643Val)	rs757827254	0.00005
NM_024741.3(ZNF408):c.377G>A (p.Ser126Asn)	rs536561101	0.00003
NM_024741.3(ZNF408):c.402A>G (p.Gln134=)	rs561320549	0.00001
NM_024741.3(ZNF408):c.130C>T (p.Pro44Ser)	rs796065315
NM_024741.3(ZNF408):c.1850C>A (p.Thr617Asn)	rs547169524
NM_024741.3(ZNF408):c.2145G>T (p.Glu715Asp)	rs796065317
NM_024741.3(ZNF408):c.694A>G (p.Met232Val)	rs796065316

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