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: rs35076622
rs35076622
2 1.000 0.040 17 45779092 intron variant G/A;C snv 0.700 1.000 2 2018 2019
dbSNP: rs12938031
rs12938031
6 0.851 0.160 17 45777136 intron variant A/G snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs143699161
rs143699161
2 17 45671346 intron variant A/G snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs1526123
rs1526123
2 1.000 0.040 17 45705974 intron variant T/C snv 0.55 0.700 1.000 1 2018 2018
dbSNP: rs1724425
rs1724425
1 17 45704381 intron variant C/T snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs17426174
rs17426174
2 17 45753572 intron variant G/C snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs35116560
rs35116560
1 17 45726820 intron variant T/C snv 0.37 0.700 1.000 1 2018 2018
dbSNP: rs3843738
rs3843738
1 17 45661828 intron variant A/G snv 0.37 0.700 1.000 1 2018 2018