ClinVar Miner

Variants studied for sick sinus syndrome 3, susceptibility to

Included ClinVar conditions (4):
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 risk factor total
0 0 193 35 7 1 236

Gene and significance breakdown #

Total genes and gene combinations: 3
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Gene or gene combination uncertain significance likely benign benign risk factor total
MYH6 146 30 5 1 182
LOC114827851, MYH6 28 2 0 0 30
LOC126861896, MYH6 19 3 2 0 24

Submitter and significance breakdown #

Total submitters: 8
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Submitter uncertain significance likely benign benign risk factor total
Fulgent Genetics, Fulgent Genetics 188 35 7 0 230
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 3 0 0 0 3
OMIM 0 0 0 1 1
MGZ Medical Genetics Center 1 0 0 0 1
Division of Human Genetics, Children's Hospital of Philadelphia 1 0 0 0 1
Juno Genomics, Hangzhou Juno Genomics, Inc 1 0 0 0 1
New York Genome Center 1 0 0 0 1
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein 1 0 0 0 1

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