ClinVar Miner

List of variants reported as pathogenic for atrial fibrillation (disease) by Fulgent Genetics,Fulgent Genetics

Included ClinVar conditions (28):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 10
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HGVS dbSNP
NM_000335.4(SCN5A):c.1099C>T (p.Arg367Cys) rs199473097
NM_000335.4(SCN5A):c.5869C>T (p.Arg1957Ter) rs757532106
NM_000335.4(SCN5A):c.665G>A (p.Arg222Gln) rs45546039
NM_000891.2(KCNJ2):c.199C>T (p.Arg67Trp) rs104894580
NM_001037.5(SCN1B):c.254G>A (p.Arg85His) rs16969925
NM_181798.1(KCNQ1):c.1207C>T (p.Gln403Ter) rs397508097
NM_181798.1(KCNQ1):c.1234C>T (p.Arg412Trp) rs199472795
NM_181798.1(KCNQ1):c.311G>A (p.Arg104His) rs199472709
NM_181798.1(KCNQ1):c.424G>A (p.Gly142Ser) rs120074193
NM_181798.1(KCNQ1):c.704A>G (p.Lys235Arg) rs12720458

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