ClinVar Miner

List of variants reported as not provided for atrial fibrillation by Cardiovascular Biomedical Research Unit, Royal Brompton & Harefield NHS Foundation Trust

Included ClinVar conditions (49):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_000335.5(SCN5A):c.1333C>G (p.His445Asp) rs199473112 0.00011
NM_000891.3(KCNJ2):c.277G>A (p.Val93Ile) rs147750704 0.00007
NM_000335.5(SCN5A):c.1282G>A (p.Glu428Lys) rs199473111 0.00006
NM_172201.2(KCNE2):c.79C>T (p.Arg27Cys) rs74315449 0.00006
NM_000335.5(SCN5A):c.5958C>A (p.Asn1986Lys) rs199473335 0.00004
NM_000335.5(SCN5A):c.3389C>T (p.Thr1130Ile) rs199473197 0.00003
NM_000335.5(SCN5A):c.1410C>G (p.Asn470Lys) rs199473115 0.00002
NM_000335.5(SCN5A):c.1963G>A (p.Glu655Lys) rs199473579 0.00001
NM_000335.5(SCN5A):c.414G>A (p.Met138Ile) rs199473060 0.00001
NM_000335.5(SCN5A):c.5473C>T (p.Arg1825Cys) rs199473635 0.00001
NM_000218.3(KCNQ1):c.418A>G (p.Ser140Gly) rs120074192
NM_000218.3(KCNQ1):c.421G>A (p.Val141Met) rs199472687
NM_000218.3(KCNQ1):c.440A>G (p.Gln147Arg) rs199472689
NM_000218.3(KCNQ1):c.625T>C (p.Ser209Pro) rs199472705
NM_000335.5(SCN5A):c.5621T>C (p.Met1874Thr) rs199473324
NM_000335.5(SCN5A):c.5848G>A (p.Val1950Met) rs41315493
NM_172201.2(KCNE2):c.269A>G (p.Glu90Gly) rs199473366

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