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: rs11672966
rs11672966
1 1.000 0.040 19 23095699 intron variant G/A snv 6.1E-02 0.700 1.000 1 2017 2017
dbSNP: rs1473419
rs1473419
1 1.000 0.040 19 23101548 intron variant C/T snv 0.54 0.700 1.000 1 2017 2017
dbSNP: rs1693286
rs1693286
1 1.000 0.040 19 23096201 intron variant C/A;G;T snv 0.15 0.700 1.000 1 2017 2017
dbSNP: rs1693294
rs1693294
1 1.000 0.040 19 23094893 intron variant C/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs2035172
rs2035172
1 1.000 0.040 19 23121702 intron variant T/C snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs2169589
rs2169589
1 1.000 0.040 19 23124334 intron variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs2219721
rs2219721
1 1.000 0.040 19 23118339 intron variant A/C;T snv 0.700 1.000 1 2017 2017
dbSNP: rs6511404
rs6511404
1 1.000 0.040 19 23105059 intron variant G/A snv 0.98 0.700 1.000 1 2017 2017
dbSNP: rs7507433
rs7507433
1 1.000 0.040 19 23121779 intron variant G/A snv 0.98 0.700 1.000 1 2017 2017
dbSNP: rs771359
rs771359
1 1.000 0.040 19 23078423 intron variant C/T snv 0.36 0.700 1.000 1 2017 2017
dbSNP: rs771362
rs771362
1 1.000 0.040 19 23076823 intron variant A/C snv 0.29 0.700 1.000 1 2017 2017