Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1013940
rs1013940
SLC5A7
0.010 GeneticVariation BEFREE ADME analyses identified associations between VIPN and ABCC1 rs3784867 (P = 5.34 × 10<sup>-5</sup> ; OR = 4.9), and SLC5A7 rs1013940 (P = 9.00 × 10<sup>-4</sup> ; OR= 8.6); genes involved in vincristine transport and inherited neuropathies, respectively. 29999516

2019
dbSNP: rs3784867
rs3784867
ABCC1
0.010 GeneticVariation BEFREE ADME analyses identified associations between VIPN and ABCC1 rs3784867 (P = 5.34 × 10<sup>-5</sup> ; OR = 4.9), and SLC5A7 rs1013940 (P = 9.00 × 10<sup>-4</sup> ; OR= 8.6); genes involved in vincristine transport and inherited neuropathies, respectively. 29999516

2019
dbSNP: rs80359890
rs80359890
SH3TC2
0.010 GeneticVariation BEFREE In addition, next generation sequencing of 52 genes for hereditary neuropathies revealed a heterozygous missense mutation c.505T > C; p.Y169H in the SH3TC2 gene that was transmitted by the healthy father. 26794302

2016
dbSNP: rs116840817
rs116840817
GJB1
0.010 GeneticVariation BEFREE The S49P mutation in the connexin 32 gene can produce aspects of a demyelinating type of X-linked hereditary neuropathy. 12207932

2002