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: rs116264287
rs116264287
1 1.000 0.080 14 68221985 intron variant C/T snv 0.700 1.000 1 2012 2012
dbSNP: rs1274646
rs1274646
1 1.000 0.080 14 68206672 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1274652
rs1274652
1 1.000 0.080 14 68209803 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1274655
rs1274655
1 1.000 0.080 14 68211261 intron variant G/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1274656
rs1274656
1 1.000 0.080 14 68212764 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1274661
rs1274661
1 1.000 0.080 14 68222502 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1298340
rs1298340
1 1.000 0.080 14 68210775 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs1316170
rs1316170
1 1.000 0.080 14 68231755 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1958113
rs1958113
1 1.000 0.080 14 68171189 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2255767
rs2255767
1 1.000 0.080 14 68196720 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2588818
rs2588818
1 1.000 0.080 14 68163861 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2588827
rs2588827
1 1.000 0.080 14 68147724 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2767378
rs2767378
1 1.000 0.080 14 68196549 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs2767382
rs2767382
1 1.000 0.080 14 68177329 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2767384
rs2767384
1 1.000 0.080 14 68169994 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1314914
rs1314914
1 1.000 0.080 14 68236359 non coding transcript exon variant C/T snv 0.13 0.700 1.000 1 2012 2012
dbSNP: rs1314913
rs1314913
1 0.807 0.120 14 68232877 intron variant C/T snv 0.13 0.830 1.000 1 2012 2019
dbSNP: rs1274640
rs1274640
1 1.000 0.080 14 68201811 intron variant C/T snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs1274643
rs1274643
1 1.000 0.080 14 68206362 intron variant T/C snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs1274648
rs1274648
1 1.000 0.080 14 68207168 intron variant T/C snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs1274638
rs1274638
1 1.000 0.080 14 68200005 intron variant T/C snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs1316118
rs1316118
1 1.000 0.080 14 68233380 intron variant T/C snv 0.16 0.700 1.000 1 2012 2012
dbSNP: rs725453
rs725453
1 1.000 0.080 14 68209141 intron variant C/T snv 0.16 0.700 1.000 1 2012 2012
dbSNP: rs1296527
rs1296527
1 1.000 0.080 14 68218743 intron variant T/C snv 0.16 0.700 1.000 1 2012 2012
dbSNP: rs1274650
rs1274650
1 1.000 0.080 14 68209456 intron variant G/A snv 0.17 0.700 1.000 1 2012 2012