Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7439366
rs7439366
0.752 0.320 4 69098620 missense variant T/C snv 0.56 0.57
CUI: C0030193
Disease: Pain
Pain
Pathological Conditions, Signs and Symptoms 0.020 1.000 2 2018 2018
dbSNP: rs4587017
rs4587017
4 69081680 intron variant T/G snv 0.63
CUI: C0030193
Disease: Pain
Pain
Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2018 2018
dbSNP: rs749415280
rs749415280
1.000 0.120 4 69096638 missense variant A/G snv
CUI: C0030193
Disease: Pain
Pain
Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2015 2015
dbSNP: rs765502022
rs765502022
0.827 0.240 4 69112695 missense variant T/C snv 1.6E-05
CUI: C0030193
Disease: Pain
Pain
Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2018 2018
dbSNP: rs773030005
rs773030005
1.000 0.040 4 69107204 synonymous variant A/C;G snv 4.0E-06; 6.8E-05
CUI: C0030193
Disease: Pain
Pain
Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2019 2019