abnormal touch/ nociception
98
significant genes8.30%
of tested genes1181
tested genesDescription
change in the ability to sense contact with objects or in the ability to sense pain, most often registered by mechanoreceptors in the skin and mucous membranes
Significant gene-phenotype associationsView data
IMPC Gene variants with abnormal touch/ nociception
Number of significant genotype-phenotype associations: 0
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Most significant associations for abnormal touch/ nociception
Not significant Significant Manual associations
Significant P-Value threshold (P < 0.0001)
Significant P-Value threshold (P < 0.0001)