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: rs1062630
rs1062630
1 6 31170330 synonymous variant G/A snv 0.18 0.22 0.700 1.000 1 2017 2017
dbSNP: rs10885
rs10885
1 6 31636814 missense variant C/T snv 0.14 0.17 0.700 1.000 1 2013 2013
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: rs12154141
rs12154141
1 6 62460168 downstream gene variant A/C snv 0.20 0.700 1.000 1 2017 2017
dbSNP: rs138117677
rs138117677
1 16 3348899 TF binding site variant GGGACT/- delins 2.8E-02 0.700 1.000 1 2017 2017
dbSNP: rs200655768
rs200655768
1 2 178711222 synonymous variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs200688486
rs200688486
1 6 32621223 regulatory region variant -/T delins 0.700 1.000 1 2013 2013
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: rs2294884
rs2294884
1 6 32399482 intron variant T/A;G snv 0.18 0.700 1.000 1 2013 2013
dbSNP: rs28362680
rs28362680
1 6 32403039 missense variant G/A snv 0.14 0.12 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: 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: rs314879
rs314879
1 13 22735243 intergenic variant C/T snv 0.78 0.700 1.000 1 2017 2017
dbSNP: rs5861895
rs5861895
1 4 129344228 regulatory region variant TT/-;T;TTT delins 0.700 1.000 1 2017 2017
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: rs80274284
rs80274284
1 1 116037356 missense variant G/T snv 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
dbSNP: rs9271488
rs9271488
1 6 32621223 regulatory region variant G/T snv 0.27 0.700 1.000 1 2013 2013
dbSNP: rs9368726
rs9368726
1 6 32470765 intron variant T/C snv 0.29 0.700 1.000 1 2013 2013