ClinVar Miner

List of variants reported as uncertain significance for Brugada syndrome 8 by Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues

Included ClinVar conditions (3):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_005477.3(HCN4):c.2782C>G (p.Pro928Ala)	rs1482640658
NM_005477.3(HCN4):c.3014C>T (p.Ser1005Phe)	rs780624939
NM_005477.3(HCN4):c.67G>A (p.Ala23Thr)	rs868045953

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