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: rs11651239
rs11651239
1 1.000 0.040 17 37139167 intron variant G/A snv 0.20 0.700 1.000 1 2017 2017
dbSNP: rs12449696
rs12449696
1 1.000 0.040 17 37095363 intron variant C/T snv 0.22 0.700 1.000 1 2017 2017
dbSNP: rs12450937
rs12450937
1 1.000 0.040 17 37137586 intron variant C/T snv 0.51 0.700 1.000 1 2017 2017
dbSNP: rs17573357
rs17573357
1 1.000 0.040 17 37119704 intron variant A/G snv 8.5E-02 0.700 1.000 1 2017 2017
dbSNP: rs1900101
rs1900101
1 1.000 0.040 17 37098342 intron variant T/G snv 0.30 0.700 1.000 1 2017 2017
dbSNP: rs2106772
rs2106772
1 1.000 0.040 17 37104485 intron variant C/T snv 0.24 0.700 1.000 1 2017 2017
dbSNP: rs7208415
rs7208415
1 1.000 0.040 17 37132758 intron variant G/A snv 0.17 0.700 1.000 1 2017 2017
dbSNP: rs7215365
rs7215365
1 1.000 0.040 17 37118979 intron variant C/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs9897583
rs9897583
1 1.000 0.040 17 37113716 intron variant C/G snv 0.34 0.700 1.000 1 2017 2017