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: rs10399681
rs10399681
1 1.000 0.040 1 158555761 upstream gene variant G/A snv 0.50 0.700 1.000 1 2017 2017
dbSNP: rs10429895
rs10429895
1 1.000 0.040 1 190689509 intron variant C/T snv 0.32 0.700 1.000 1 2017 2017
dbSNP: rs10489202
rs10489202
2 0.925 0.080 1 167933841 intron variant G/T snv 0.20 0.700 1.000 1 2017 2017
dbSNP: rs10489573
rs10489573
1 1.000 0.040 1 18358708 intron variant C/T snv 0.21 0.700 1.000 1 2017 2017
dbSNP: rs10489676
rs10489676
1 1.000 0.040 1 157650099 intergenic variant T/C snv 0.24 0.700 1.000 1 2017 2017
dbSNP: rs10493240
rs10493240
1 1.000 0.040 1 58318478 intron variant G/C;T snv 0.700 1.000 1 2017 2017
dbSNP: rs10493241
rs10493241
1 1.000 0.040 1 58318299 intron variant G/A snv 0.13 0.700 1.000 1 2017 2017
dbSNP: rs10493249
rs10493249
1 1.000 0.040 1 58306455 intron variant G/T snv 0.14 0.700 1.000 1 2017 2017
dbSNP: rs10493260
rs10493260
1 1.000 0.040 1 59112910 intron variant T/C snv 0.11 0.700 1.000 1 2017 2017
dbSNP: rs10494164
rs10494164
1 1.000 0.040 1 114003906 intron variant A/G snv 6.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs10494229
rs10494229
1 1.000 0.040 1 119686494 intron variant A/G snv 0.23 0.700 1.000 1 2017 2017
dbSNP: rs10494504
rs10494504
1 1.000 0.040 1 177768254 intron variant A/G snv 0.18 0.700 1.000 1 2017 2017
dbSNP: rs10494541
rs10494541
1 1.000 0.040 1 181581329 intron variant A/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs10494629
rs10494629
1 1.000 0.040 1 190028800 intergenic variant A/C snv 3.4E-02 0.700 1.000 1 2017 2017
dbSNP: rs10494915
rs10494915
1 1.000 0.040 1 209068535 intergenic variant A/G snv 0.16 0.700 1.000 1 2017 2017
dbSNP: rs10494916
rs10494916
1 1.000 0.040 1 209072514 intergenic variant T/G snv 0.38 0.700 1.000 1 2017 2017
dbSNP: rs1060041
rs1060041
1 1.000 0.040 1 168004738 synonymous variant C/T snv 0.25 0.20 0.700 1.000 1 2017 2017
dbSNP: rs10754479
rs10754479
1 1.000 0.040 1 245847731 intron variant T/C snv 0.40 0.700 1.000 1 2017 2017
dbSNP: rs10754699
rs10754699
1 1.000 0.040 1 240386016 intron variant C/T snv 0.46 0.700 1.000 1 2017 2017
dbSNP: rs10789075
rs10789075
1 1.000 0.040 1 59116876 intron variant A/T snv 0.35 0.700 1.000 1 2017 2017
dbSNP: rs10797729
rs10797729
1 1.000 0.040 1 181570611 intron variant G/A snv 0.23 0.700 1.000 1 2017 2017
dbSNP: rs10797732
rs10797732
1 1.000 0.040 1 181576364 intron variant G/T snv 0.23 0.700 1.000 1 2017 2017
dbSNP: rs10798906
rs10798906
1 1.000 0.040 1 29874731 intergenic variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs10798928
rs10798928
1 1.000 0.040 1 29944713 intergenic variant C/T snv 0.74 0.700 1.000 1 2017 2017
dbSNP: rs10800238
rs10800238
1 1.000 0.040 1 166487150 intron variant T/C;G snv 0.58 0.700 1.000 1 2017 2017