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: rs4946935
rs4946935
2 1.000 0.040 6 108679539 intron variant A/G snv 0.54 0.700 1.000 2 2018 2019
dbSNP: rs2022464
rs2022464
1 6 108624167 intron variant A/C;T snv 0.56 0.700 1.000 1 2019 2019
dbSNP: rs2490272
rs2490272
1 6 108574183 intron variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs3813498
rs3813498
2 6 108622962 intron variant C/T snv 0.71 0.700 1.000 1 2018 2018
dbSNP: rs4945816
rs4945816
2 1.000 0.040 6 108680839 3 prime UTR variant C/T snv 0.53 0.700 1.000 1 2019 2019
dbSNP: rs9285397
rs9285397
1 6 108630452 intron variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs9398173
rs9398173
1 6 108679113 intron variant T/C snv 0.55 0.700 1.000 1 2018 2018