List of variants in gene GATAD1 reported as likely benign for Cardiovascular phenotype

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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: 18

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HGVS	dbSNP	gnomAD frequency
NM_021167.5(GATAD1):c.276T>G (p.Ser92=)	rs143082866	0.00021
NM_021167.5(GATAD1):c.558G>A (p.Thr186=)	rs141932124	0.00008
NM_021167.5(GATAD1):c.591C>T (p.Asp197=)	rs1031781653	0.00006
NM_021167.5(GATAD1):c.681T>A (p.Ser227=)	rs759247482	0.00004
NM_021167.5(GATAD1):c.603C>T (p.Pro201=)	rs150863199	0.00003
NM_021167.5(GATAD1):c.285C>T (p.Leu95=)	rs371500622	0.00001
NM_021167.5(GATAD1):c.367T>C (p.Leu123=)	rs146142781	0.00001
NM_021167.5(GATAD1):c.507A>G (p.Gln169=)	rs775915716	0.00001
NM_021167.5(GATAD1):c.774A>G (p.Ala258=)	rs775303568	0.00001
NM_021167.5(GATAD1):c.354A>G (p.Arg118=)
NM_021167.5(GATAD1):c.408A>T (p.Ile136=)
NM_021167.5(GATAD1):c.564C>T (p.Leu188=)
NM_021167.5(GATAD1):c.570T>C (p.Pro190=)
NM_021167.5(GATAD1):c.609C>T (p.Ser203=)
NM_021167.5(GATAD1):c.620-4C>T
NM_021167.5(GATAD1):c.702A>G (p.Ser234=)
NM_021167.5(GATAD1):c.738G>A (p.Lys246=)
NM_021167.5(GATAD1):c.798C>A (p.Ala266=)	rs2115886142

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