Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs5443
rs5443
GNB3 ; CDCA3
106 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.030 1.000 3 2004 2011
dbSNP: rs1256318228
rs1256318228
PTGS1
1 9 122386588 synonymous variant C/T snv 7.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs211105
rs211105
TPH1
4 1.000 11 18033757 intron variant T/G snv 0.19 0.010 1.000 1 2018 2018
dbSNP: rs222747
rs222747
TRPV1
8 0.827 0.240 17 3589906 missense variant C/A;G;T snv 0.72; 4.5E-06 0.010 1.000 1 2014 2014
dbSNP: rs4836884
rs4836884
PTGS1
1 9 122383715 synonymous variant C/G;T snv 4.0E-06; 2.8E-03 0.010 1.000 1 2011 2011