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: rs10761733
rs10761733
1 10 63275024 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs10761739
rs10761739
1 10 63302248 intron variant G/C snv 0.38 0.700 1.000 1 2019 2019
dbSNP: rs10761765
rs10761765
1 10 63429213 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10995505
rs10995505
1 10 63331399 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2393967
rs2393967
3 10 63373396 intron variant A/C snv 0.23 0.700 1.000 1 2018 2018
dbSNP: rs4745706
rs4745706
1 10 63399820 intron variant T/C snv 0.13 0.700 1.000 1 2019 2019
dbSNP: rs6479901
rs6479901
1 10 63421016 intron variant C/A snv 0.66 0.700 1.000 1 2019 2019
dbSNP: rs7896518
rs7896518
5 10 63344740 intron variant A/G snv 0.38 0.700 1.000 1 2017 2017
dbSNP: rs7924036
rs7924036
3 10 63431885 intron variant G/A;T snv 0.700 1.000 1 2018 2018