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: rs12937080
rs12937080
1 1.000 0.120 17 61852376 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs34289250
rs34289250
2 0.925 0.120 17 61803285 intron variant T/C snv 7.8E-03 0.700 1.000 1 2011 2011
dbSNP: rs1064795649
rs1064795649
2 1.000 0.120 17 61799205 frameshift variant CT/- delins 0.700 0
dbSNP: rs1199923024
rs1199923024
1 1.000 0.120 17 61683945 missense variant G/A snv 1.6E-05 7.0E-06 0.700 0
dbSNP: rs137852986
rs137852986
13 0.732 0.440 17 61716051 stop gained G/A snv 1.7E-04 1.5E-04 0.700 0
dbSNP: rs2191249
rs2191249
3 0.882 0.120 17 61758503 intron variant T/G snv 0.79 0.010 1.000 1 2007 2007
dbSNP: rs4988344
rs4988344
4 0.882 0.120 17 61847251 intron variant G/C snv 0.20 0.15 0.010 1.000 1 2007 2007