ClinVar Miner

Variants from KTest Genetics, KTest

Location: Vietnam  Primary collection method: clinical testing
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
34 22 0 0 0 56

Gene and significance breakdown #

Total genes and gene combinations: 24
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Gene or gene combination pathogenic likely pathogenic total
TTN 14 5 19
DSP 2 1 3
LOC126806424, TTN 2 1 3
TPM1 1 2 3
DES 0 2 2
FKTN 2 0 2
LAMP2 1 1 2
LMNA 1 1 2
LOC126806423, TTN 2 0 2
MYBPC3 0 2 2
MYH7 2 0 2
TNNT2 2 0 2
ACTC1, GJD2-DT 0 1 1
BAG3 1 0 1
CEP85L, PLN 1 0 1
DMD 1 0 1
LAMA2 0 1 1
LOC126861897, MHRT, MYH7 0 1 1
LOC129992585, SGCB 1 0 1
MYH6 0 1 1
RBM20 1 0 1
SDHA 0 1 1
TBX5 0 1 1
TCAP 0 1 1

Condition and significance breakdown #

Total conditions: 17
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Condition pathogenic likely pathogenic total
Dilated cardiomyopathy 1G 18 6 24
Primary dilated cardiomyopathy 2 4 6
Cardiomyopathy, dilated, with wooly hair, keratoderma, and tooth agenesis 2 1 3
Dilated cardiomyopathy 1S 2 1 3
Dilated cardiomyopathy 1Y 1 2 3
Dilated cardiomyopathy 1A 1 1 2
Dilated cardiomyopathy 1D 2 0 2
Dilated cardiomyopathy 1I 0 2 2
Dilated cardiomyopathy 1X 2 0 2
Left ventricular noncompaction 10 0 2 2
Dilated cardiomyopathy 1DD 1 0 1
Dilated cardiomyopathy 1EE 0 1 1
Dilated cardiomyopathy 1GG 0 1 1
Dilated cardiomyopathy 1HH 1 0 1
Dilated cardiomyopathy 1P 1 0 1
Dilated cardiomyopathy 1R 0 1 1
Dilated cardiomyopathy 3B 1 0 1

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