ClinVar Miner

Variants studied for Spastic paraplegia, autosomal dominant

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 0 216 192 57 465

Gene and significance breakdown #

Total genes and gene combinations: 11
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Gene or gene combination uncertain significance likely benign benign total
NIPA1 47 38 15 100
SPAST 38 33 4 75
REEP1 20 20 10 50
ZFYVE27 17 21 9 47
WASHC5 15 24 6 45
KIF5A 27 15 1 43
SLC33A1 19 14 4 37
ATL1 12 12 4 28
HSPD1 13 11 4 28
RTN2 7 4 0 11
ATL1, MAP4K5 1 0 0 1

Submitter and significance breakdown #

Total submitters: 1
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Submitter uncertain significance likely benign benign total
Illumina Clinical Services Laboratory,Illumina 216 192 57 465

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