ClinVar Miner

Variants studied for Wolff-Parkinson-white syndrome (disease)

Included ClinVar conditions (5):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign total
4 18 150 14 10 195

Gene and significance breakdown #

Total genes and gene combinations: 49
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
PRKAG2 2 0 81 14 10 106
RYR2 0 0 7 0 0 7
RHBDF1 0 0 5 0 0 5
MYBPC3 0 1 3 0 0 4
PRDM16 0 0 4 0 0 4
ANK2 0 0 3 0 0 3
JUP 0 1 2 0 0 3
KCNQ1 0 2 1 0 0 3
MYH7 0 2 1 0 0 3
VCL 0 0 3 0 0 3
ABCC9 0 1 1 0 0 2
ACTC1, LOC101928174 0 1 1 0 0 2
AKAP9 0 0 2 0 0 2
CACNA1C 0 0 2 0 0 2
DPP6 0 0 2 0 0 2
DSP 0 0 2 0 0 2
FLNC 0 0 2 0 0 2
FNIP1 0 0 2 0 0 2
KCNH2 0 0 2 0 0 2
LAMA4 0 0 2 0 0 2
MYH6 0 1 1 0 0 2
SCN5A 0 2 0 0 0 2
TNNT2 0 2 0 0 0 2
TTC39A 0 0 2 0 0 2
TTN 0 2 0 0 0 2
ACTN2 0 0 1 0 0 1
CACNA1E 0 0 1 0 0 1
CASQ2 0 1 0 0 0 1
COL5A1 0 0 1 0 0 1
FLNA 0 0 1 0 0 1
GJA5 0 0 1 0 0 1
GPD1L 0 0 1 0 0 1
KCNJ2 0 0 1 0 0 1
LAMC1 0 0 1 0 0 1
LMNA 0 0 1 0 0 1
MHRT, MYH7 0 1 0 0 0 1
MYH11, NDE1 0 0 1 0 0 1
NEBL 0 0 1 0 0 1
NODAL 1 0 0 0 0 1
PITX2 0 0 1 0 0 1
RBM20 0 0 1 0 0 1
SLC26A4 0 1 0 0 0 1
SNTA1 0 0 1 0 0 1
TBX20 1 0 0 0 0 1
TBX5 0 0 1 0 0 1
TCAP 0 0 1 0 0 1
TGFBR2 0 0 1 0 0 1
TRPM4 0 0 1 0 0 1
WWP1 0 0 1 0 0 1

Submitter and significance breakdown #

Total submitters: 10
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Illumina Clinical Services Laboratory,Illumina 0 0 78 14 10 102
Lupski Lab, Baylor-Hopkins CMG, Baylor College of Medicine 1 15 69 0 0 85
Fulgent Genetics,Fulgent Genetics 0 0 2 0 0 2
Agnes Ginges Centre for Molecular Cardiology,Centenary Institute 0 2 0 0 0 2
OMIM 1 0 0 0 0 1
Clinical Molecular Genetics Laboratory,Johns Hopkins All Children's Hospital 0 1 0 0 0 1
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology 1 0 0 0 0 1
Centre for Genomic and Experimental Medicine,University of Edinburgh 1 0 0 0 0 1
Soonchunhyang University Bucheon Hospital,Soonchunhyang University Medical Center 0 0 1 0 0 1
Centre for Mendelian Genomics,University Medical Centre Ljubljana 0 0 1 0 0 1

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