ClinVar Miner

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

Included ClinVar conditions (28):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 17
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HGVS dbSNP
NM_000335.4(SCN5A):c.1282G>A (p.Glu428Lys) rs199473111
NM_000335.4(SCN5A):c.1333C>G (p.His445Asp) rs199473112
NM_000335.4(SCN5A):c.1410C>G (p.Asn470Lys) rs199473115
NM_000335.4(SCN5A):c.1963G>A (p.Glu655Lys) rs199473579
NM_000335.4(SCN5A):c.3389C>T (p.Thr1130Ile) rs199473197
NM_000335.4(SCN5A):c.414G>A (p.Met138Ile) rs199473060
NM_000335.4(SCN5A):c.5473C>T (p.Arg1825Cys) rs199473635
NM_000335.4(SCN5A):c.5621T>C (p.Met1874Thr) rs199473324
NM_000335.4(SCN5A):c.5848G>A (p.Val1950Met) rs41315493
NM_000335.4(SCN5A):c.5958C>A (p.Asn1986Lys) rs199473335
NM_000891.2(KCNJ2):c.277G>A (p.Val93Ile) rs147750704
NM_172201.1(KCNE2):c.269A>G (p.Glu90Gly) rs199473366
NM_172201.1(KCNE2):c.79C>T (p.Arg27Cys) rs74315449
NM_181798.1(KCNQ1):c.244T>C (p.Ser82Pro) rs199472705
NM_181798.1(KCNQ1):c.37A>G (p.Ser13Gly) rs120074192
NM_181798.1(KCNQ1):c.40G>A (p.Val14Met) rs199472687
NM_181798.1(KCNQ1):c.59A>G (p.Gln20Arg) rs199472689

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