ClinVar Miner

List of variants reported as uncertain significance for Atrial fibrillation, familial, 6

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Total variants: 34
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HGVS dbSNP
NC_000001.11:g.(?_11012634)_(11934865_?)del
NM_006172.4(NPPA):c.103G>A (p.Ala35Thr)
NM_006172.4(NPPA):c.112A>G (p.Met38Val) rs764360980
NM_006172.4(NPPA):c.118T>C (p.Phe40Leu)
NM_006172.4(NPPA):c.149A>T (p.Lys50Met)
NM_006172.4(NPPA):c.154C>T (p.Pro52Ser)
NM_006172.4(NPPA):c.16ACC[2] (p.Thr8del)
NM_006172.4(NPPA):c.172G>A (p.Val58Met) rs768114654
NM_006172.4(NPPA):c.176C>T (p.Pro59Leu) rs759999149
NM_006172.4(NPPA):c.197C>T (p.Pro66Leu) rs150794709
NM_006172.4(NPPA):c.19A>G (p.Thr7Ala)
NM_006172.4(NPPA):c.206A>C (p.Glu69Ala) rs376184349
NM_006172.4(NPPA):c.208G>T (p.Ala70Ser) rs1433555315
NM_006172.4(NPPA):c.219_227del (p.Ser75_Leu77del) rs1557442938
NM_006172.4(NPPA):c.23C>T (p.Thr8Ile) rs142653342
NM_006172.4(NPPA):c.253G>A (p.Gly85Arg) rs749353276
NM_006172.4(NPPA):c.25G>A (p.Val9Met)
NM_006172.4(NPPA):c.277_278del (p.Asp93fs) rs774165756
NM_006172.4(NPPA):c.316G>C (p.Asp106His)
NM_006172.4(NPPA):c.319C>T (p.Arg107Ter)
NM_006172.4(NPPA):c.337A>G (p.Ser113Gly)
NM_006172.4(NPPA):c.338G>C (p.Ser113Thr)
NM_006172.4(NPPA):c.346_354del (p.Arg116_Leu118del)
NM_006172.4(NPPA):c.350C>T (p.Ala117Val) rs72639212
NM_006172.4(NPPA):c.367C>A (p.Arg123=) rs377057675
NM_006172.4(NPPA):c.368G>A (p.Arg123Gln)
NM_006172.4(NPPA):c.370A>G (p.Ser124Gly) rs1215729892
NM_006172.4(NPPA):c.377G>A (p.Arg126Gln) rs1803268
NM_006172.4(NPPA):c.425G>A (p.Ser142Asn) rs781197146
NM_006172.4(NPPA):c.449G>A (p.Arg150Gln) rs202102042
NM_006172.4(NPPA):c.59T>C (p.Leu20Pro)
NM_006172.4(NPPA):c.78T>A (p.Asn26Lys) rs770401799
NM_006172.4(NPPA):c.85T>C (p.Tyr29His) rs771777356
NM_006172.4(NPPA):c.89A>G (p.Asn30Ser)

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