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: rs1003643
rs1003643
1 1.000 0.080 22 39280489 downstream gene variant T/G snv 0.34 0.700 1.000 1 2011 2011
dbSNP: rs1003644
rs1003644
1 1.000 0.080 22 39280739 downstream gene variant G/A snv 0.31 0.700 1.000 1 2011 2011
dbSNP: rs1005999
rs1005999
1 1.000 0.080 2 104907333 intron variant C/T snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs1008591
rs1008591
1 1.000 0.080 19 46227357 upstream gene variant A/G snv 0.45 0.700 1.000 1 2012 2012
dbSNP: rs1008723
rs1008723
3 0.925 0.160 17 39910014 intron variant G/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1011082
rs1011082
1 1.000 0.080 17 39912261 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs1015092
rs1015092
1 1.000 0.080 20 8769415 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10168266
rs10168266
8 0.776 0.400 2 191071078 intron variant C/T snv 0.19 0.710 1.000 2 2014 2017
dbSNP: rs10174098
rs10174098
3 0.882 0.200 2 186628015 intron variant G/A snv 0.62 0.010 1.000 1 2011 2011
dbSNP: rs10181656
rs10181656
9 0.763 0.360 2 191105153 intron variant G/C snv 0.79 0.010 1.000 1 2014 2014
dbSNP: rs1019212
rs1019212
1 1.000 0.080 19 46225962 upstream gene variant G/A snv 0.45 0.700 1.000 1 2012 2012
dbSNP: rs10234405
rs10234405
1 1.000 0.080 7 4034827 intron variant A/G snv 0.33 0.700 1.000 1 2012 2012
dbSNP: rs10237319
rs10237319
1 1.000 0.080 7 4033969 intron variant C/T snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs10237488
rs10237488
1 1.000 0.080 7 4034710 intron variant T/G snv 0.33 0.700 1.000 1 2012 2012
dbSNP: rs10237838
rs10237838
1 1.000 0.080 7 4034366 intron variant C/T snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs10265937
rs10265937
1 1.000 0.080 7 4034017 intron variant G/A snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs10266101
rs10266101
1 1.000 0.080 7 4034187 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10278187
rs10278187
1 1.000 0.080 7 4034741 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1031458
rs1031458
1 1.000 0.080 17 39915920 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10415976
rs10415976
1 1.000 0.080 19 941603 intron variant A/G snv 0.18 0.700 1.000 1 2017 2017
dbSNP: rs10445308
rs10445308
5 0.851 0.240 17 39781794 intron variant C/T snv 0.38 0.700 1.000 1 2012 2012
dbSNP: rs10445337
rs10445337
3 0.925 0.120 17 45990034 missense variant T/C snv 0.15 0.15 0.700 1.000 1 2012 2012
dbSNP: rs10445371
rs10445371
3 0.925 0.120 17 45988044 intron variant G/A snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs1045642
rs1045642
214 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2005 2005
dbSNP: rs10485860
rs10485860
1 1.000 0.080 7 4050651 intron variant T/C snv 0.25 0.700 1.000 1 2012 2012