ClinVar Miner

Variants studied for Huntington disease

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 other total
3 0 0 0 2 2 7

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic benign other total
HTT, LOC109461479 3 1 0 4
HTT 0 1 2 3

Submitter and significance breakdown #

Total submitters: 3
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Submitter pathogenic benign other total
GeneReviews 3 1 0 4
American College of Medical Genetics and Genomics (ACMG) 1 1 2 4
OMIM 1 0 0 1

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