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: rs2236225
rs2236225
52 0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 0.100 0.857 14 2002 2019
dbSNP: rs1256146
rs1256146
1 14 64453947 intron variant G/A snv 0.17 0.010 1.000 1 2015 2015
dbSNP: rs17857382
rs17857382
1 14 64449470 missense variant C/G;T snv 4.0E-06; 7.6E-03 0.010 < 0.001 1 2015 2015
dbSNP: rs1950902
rs1950902
11 0.776 0.240 14 64415662 missense variant A/G snv 0.83 0.83 0.010 < 0.001 1 2015 2015
dbSNP: rs56811449
rs56811449
1 14 64417358 intron variant C/T snv 0.16 0.010 1.000 1 2015 2015
dbSNP: rs6573559
rs6573559
1 14 64456448 intron variant G/T snv 0.31 0.010 1.000 1 2015 2015