ClinVar Miner

List of variants reported as uncertain significance for cardiac arrest

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 29
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HGVS dbSNP gnomAD frequency
NM_001148.6(ANK2):c.6206G>A (p.Arg2069His) rs149645600 0.00065
NM_001943.5(DSG2):c.437G>T (p.Arg146Leu) rs113451409 0.00054
NM_005751.5(AKAP9):c.1099G>A (p.Val367Met) rs138161478 0.00031
NM_001148.6(ANK2):c.5509G>A (p.Ala1837Thr) rs199527708 0.00024
NM_017636.4(TRPM4):c.1069C>T (p.Arg357Trp) rs764690335 0.00007
NM_005751.5(AKAP9):c.1067A>T (p.Asp356Val) rs533277424 0.00005
NM_201596.3(CACNB2):c.1206+3A>T rs200174877 0.00005
NM_001148.6(ANK2):c.7458C>G (p.His2486Gln) rs776972443 0.00004
NM_001943.5(DSG2):c.1063G>A (p.Ala355Thr) rs201046640 0.00004
NM_005477.3(HCN4):c.2197G>A (p.Val733Ile) rs376631391 0.00004
NM_201596.3(CACNB2):c.1642G>A (p.Gly548Ser) rs730880059 0.00004
NM_004415.4(DSP):c.2047G>A (p.Glu683Lys) rs775181391 0.00003
NM_001148.6(ANK2):c.7577C>T (p.Ser2526Leu) rs762909298 0.00002
NM_000335.5(SCN5A):c.559A>G (p.Thr187Ala) rs869025517 0.00001
NM_001035.3(RYR2):c.378T>A (p.Ser126Arg) rs869025507 0.00001
NM_002471.4(MYH6):c.4713G>T (p.Lys1571Asn) rs730880151 0.00001
NM_004415.4(DSP):c.2260G>A (p.Glu754Lys) rs730880080 0.00001
NM_004415.4(DSP):c.7249G>T (p.Asp2417Tyr) rs760501352 0.00001
NM_005751.5(AKAP9):c.11378C>G (p.Ser3793Cys) rs730880044 0.00001
NM_000335.5(SCN5A):c.5072T>C (p.Phe1691Ser) rs869025521
NM_001035.3(RYR2):c.13759A>C (p.Ile4587Leu) rs730880198
NM_001377540.1(SLMAP):c.2020+1G>A rs869025527
NM_001943.5(DSG2):c.2188A>G (p.Thr730Ala) rs780650226
NM_003803.4(MYOM1):c.3708C>A (p.Ser1236Arg) rs869025489
NM_004982.4(KCNJ8):c.83G>C (p.Arg28Pro) rs768851540
NM_005751.5(AKAP9):c.11276C>T (p.Pro3759Leu) rs869025356
NM_014000.3(VCL):c.1559G>A (p.Arg520Gln) rs757009736
NM_130797.4(DPP6):c.1039G>A (p.Ala347Thr) rs770646362
NM_201596.3(CACNB2):c.1594T>G (p.Ser532Ala) rs869025371

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