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: rs1161098
rs1161098
1 12 67453680 intron variant G/A snv 0.84 0.700 1.000 1 2017 2017
dbSNP: rs116671518
rs116671518
1 4 107189709 intron variant T/C snv 1.9E-02 0.700 1.000 1 2017 2017
dbSNP: rs12759054
rs12759054
3 1.000 0.040 1 233984064 intron variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs204992
rs204992
1 6 32189131 intron variant G/A snv 0.22 0.700 1.000 1 2013 2013
dbSNP: rs2153486
rs2153486
1 14 87737048 intron variant C/T snv 0.68 0.700 1.000 1 2017 2017
dbSNP: rs2239802
rs2239802
4 0.882 0.200 6 32444069 intron variant C/A;G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs2239803
rs2239803
4 0.882 0.240 6 32444056 intron variant C/A;T snv 0.50 0.700 1.000 1 2013 2013
dbSNP: rs2239804
rs2239804
5 0.851 0.240 6 32443746 intron variant T/A;C snv 0.51 0.700 1.000 1 2013 2013
dbSNP: rs2294881
rs2294881
3 1.000 0.040 6 32399827 intron variant T/C snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs2294882
rs2294882
2 6 32399738 intron variant T/C snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs2294884
rs2294884
1 6 32399482 intron variant T/A;G snv 0.18 0.700 1.000 1 2013 2013
dbSNP: rs2395185
rs2395185
17 0.724 0.360 6 32465390 intron variant G/T snv 0.29 0.700 1.000 1 2013 2013
dbSNP: rs2736157
rs2736157
2 1.000 0.120 6 31633043 intron variant A/G;T snv 0.15 0.17 0.700 1.000 1 2013 2013
dbSNP: rs3104369
rs3104369
1 6 32634705 intron variant T/C snv 0.71 0.700 1.000 1 2013 2013
dbSNP: rs3129888
rs3129888
4 0.882 0.240 6 32443949 intron variant G/A snv 0.82 0.80 0.700 1.000 1 2013 2013
dbSNP: rs3130048
rs3130048
3 1.000 0.120 6 31645962 intron variant T/C snv 0.23 0.700 1.000 1 2013 2013
dbSNP: rs3130070
rs3130070
1 6 31624031 intron variant A/G snv 0.17 0.700 1.000 1 2013 2013
dbSNP: rs3130623
rs3130623
1 6 31629923 intron variant C/T snv 0.18 0.700 1.000 1 2013 2013
dbSNP: rs4248166
rs4248166
2 1.000 0.040 6 32398644 intron variant T/C snv 0.18 0.700 1.000 1 2013 2013
dbSNP: rs4935356
rs4935356
2 1.000 0.080 6 32444611 intron variant T/A;G snv 0.700 1.000 1 2013 2013
dbSNP: rs594418
rs594418
1 10 82625296 intron variant G/A snv 0.83 0.700 1.000 1 2017 2017
dbSNP: rs6105452
rs6105452
1 20 15683126 intron variant C/T snv 0.10 0.700 1.000 1 2017 2017
dbSNP: rs62309385
rs62309385
1 4 136134743 intron variant G/C snv 9.8E-02 0.700 1.000 1 2017 2017
dbSNP: rs6797827
rs6797827
1 3 109735523 intron variant C/T snv 0.18 0.700 1.000 1 2017 2017
dbSNP: rs9267536
rs9267536
1 6 31683417 intron variant A/C snv 5.3E-02 0.700 1.000 1 2013 2013