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: rs1511299
rs1511299
1 3 141997230 intron variant T/C snv 0.19 0.700 1.000 2 2016 2019
dbSNP: rs10587862
rs10587862
1 3 142045613 intron variant TTTTT/-;T;TT;TTT;TTTT;TTTTTT;TTTTTTT;TTTTTTTTTTTTTTTTT delins 0.700 1.000 1 2019 2019
dbSNP: rs1397764
rs1397764
1 3 142031968 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs147877018
rs147877018
1 3 142094507 intron variant G/A snv 6.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs149064151
rs149064151
1 3 142045613 intron variant TTTTT/-;T;TT;TTT;TTTT;TTTTTT;TTTTTTT;TTTTTTTTTTTTTTTTT delins 0.700 1.000 1 2019 2019
dbSNP: rs2861422
rs2861422
2 3 142005802 intron variant C/T snv 0.29 0.700 1.000 1 2016 2016
dbSNP: rs347685
rs347685
4 1.000 0.080 3 142088295 intron variant C/A snv 0.74 0.700 1.000 1 2016 2016
dbSNP: rs6791514
rs6791514
1 3 142047463 intron variant C/G snv 0.76 0.700 1.000 1 2019 2019
dbSNP: rs7640665
rs7640665
2 3 142094330 intron variant G/A;C;T snv 0.700 1.000 1 2017 2017