ClinVar Miner

Variants studied for Hypokalemic periodic paralysis

Coded as:
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
0 0 102 145 44 291

Gene and significance breakdown #

Total genes and gene combinations: 3
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Gene or gene combination uncertain significance likely benign benign total
CACNA1S 61 75 21 157
GH-LCR, SCN4A 33 44 20 97
SCN4A 8 26 3 37

Submitter and significance breakdown #

Total submitters: 2
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Submitter uncertain significance likely benign benign total
Illumina Clinical Services Laboratory,Illumina 101 145 44 290
CSER_CC_NCGL; University of Washington Medical Center 1 0 0 1

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