paresthesia Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Abnormal sensations such as tingling, pricking, or numbness of the skin with no apparent physical cause. (Human Phenotype Ontology, HP_0003401)
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25 genes associated with the paresthesia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
CLEC12B C-type lectin domain family 12, member B 0.899912
STK32B serine/threonine kinase 32B 0.882984
STAT6 signal transducer and activator of transcription 6, interleukin-4 induced 0.882984
PPP3CA protein phosphatase 3, catalytic subunit, alpha isozyme 0.832497
SETBP1 SET binding protein 1 0.824663
METTL4 methyltransferase like 4 0.669362
PARVG parvin, gamma 0.621094
BSX brain-specific homeobox 0.6209
C20ORF27 chromosome 20 open reading frame 27 0.592654
SCNN1A sodium channel, non voltage gated 1 alpha subunit 0.589794
LOC100505718 0.582578
ELP3 elongator acetyltransferase complex subunit 3 0.580561
WDR64 WD repeat domain 64 0.566616
CHURC1 churchill domain containing 1 0.565624
ABCC9 ATP-binding cassette, sub-family C (CFTR/MRP), member 9 0.562717
LRRC4C leucine rich repeat containing 4C 0.53334
TRIM58 tripartite motif containing 58 0.522421
GLIS1 GLIS family zinc finger 1 0.518312
HYDIN HYDIN, axonemal central pair apparatus protein 0.509857
PCNT pericentrin 0.500231
RANBP9 RAN binding protein 9 0.498995
LRRTM1 leucine rich repeat transmembrane neuronal 1 0.470969
PDE1A phosphodiesterase 1A, calmodulin-dependent 0.465095
WDFY2 WD repeat and FYVE domain containing 2 0.448227
KDM4C lysine (K)-specific demethylase 4C 0.425822