ClinVar Miner

List of variants in gene HCN4 reported as benign for Cardiovascular phenotype

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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_005477.3(HCN4):c.3600A>G (p.Pro1200=) rs529004 0.88237
NM_005477.3(HCN4):c.1558C>T (p.Leu520=) rs12909882 0.07848
NM_005477.3(HCN4):c.2556G>A (p.Pro852=) rs117819825 0.04888
NM_005477.3(HCN4):c.107G>A (p.Gly36Glu) rs143090627 0.04452
NM_005477.3(HCN4):c.1839C>T (p.Phe613=) rs117731813 0.01108
NM_005477.3(HCN4):c.1683C>A (p.Gly561=) rs62641690 0.01030
NM_005477.3(HCN4):c.3337A>G (p.Met1113Val) rs142735148 0.00983
NM_005477.3(HCN4):c.3033T>G (p.Ser1011=) rs186728422 0.00931
NM_005477.3(HCN4):c.2979G>A (p.Thr993=) rs75307879 0.00796
NM_005477.3(HCN4):c.2648C>G (p.Pro883Arg) rs148398509 0.00737
NM_005477.3(HCN4):c.2673G>A (p.Ser891=) rs191092709 0.00666
NM_005477.3(HCN4):c.36C>G (p.Leu12=) rs201193660 0.00635
NM_005477.3(HCN4):c.3288C>T (p.Asp1096=) rs116042117 0.00490
NM_005477.3(HCN4):c.2831C>T (p.Ala944Val) rs144450232 0.00416
NM_005477.3(HCN4):c.2601C>A (p.Ala867=) rs143188160 0.00352
NM_005477.3(HCN4):c.2657C>T (p.Ala886Val) rs200575377 0.00352
NM_005477.3(HCN4):c.3587G>A (p.Arg1196His) rs147181577 0.00191
NM_005477.3(HCN4):c.546C>G (p.Pro182=) rs571671463 0.00122
NM_005477.3(HCN4):c.2700C>A (p.Ala900=) rs377656260

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