ClinVar Miner

Variants from Genesis Genome Database

Location: United States  Primary collection method: research
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 0 283 0 0 283

Gene and significance breakdown #

Total genes and gene combinations: 33
Download table as spreadsheet
Gene or gene combination uncertain significance total
SH3TC2 29 29
IGHMBP2 25 25
MFN2 25 25
DYNC1H1 23 23
PRX 22 22
SEPTIN9 17 17
KIF1B 16 16
GARS1 12 12
MORC2 12 12
FIG4 11 11
LITAF 11 11
NEFL 11 11
GDAP1 10 10
TRPV4 9 9
AARS1 8 8
LRSAM1 7 7
PMP22 7 7
MPZ 5 5
EGR2 4 4
HSPB1 4 4
HSPB8 2 2
RAB7A 2 2
DYNC1H1, LOC126862060 1 1
GDAP1, LOC130000622 1 1
IGHMBP2, LOC126861245 1 1
KIF1B, LOC129388446 1 1
KIF1B, LOC129388447 1 1
LOC112872299, RAB7A 1 1
LOC126860330, NEFL 1 1
LOC126862651, SEPTIN9 1 1
LOC129929426, MFN2 1 1
LOC130064454, PRX 1 1
PLD3, PRX 1 1

Condition and significance breakdown #

Total conditions: 8
Download table as spreadsheet
Condition uncertain significance total
Charcot-Marie-Tooth disease 207 207
Charcot-Marie-Tooth disease, type I 40 40
Distal spinal muscular atrophy 26 26
Charcot-Marie-Tooth disease type 4 24 24
Neuronopathy, distal hereditary motor, autosomal dominant 5 5
Charcot-Marie-Tooth disease type 5 3 3
Sodium channelopathy-related small fiber neuropathy 3 3
Autosomal dominant intermediate Charcot-Marie-Tooth disease 2 2

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.