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: rs9373124
rs9373124
3 6 135102071 intron variant T/C snv 0.33 0.800 1.000 1 2011 2011
dbSNP: rs2210366
rs2210366
4 6 135094070 intron variant G/A snv 0.34 0.700 1.000 1 2018 2018
dbSNP: rs34208856
rs34208856
6 6 135099930 intron variant TT/-;T;TTT;TTTTTTTTT delins 0.700 1.000 1 2016 2016
dbSNP: rs35959442
rs35959442
1 6 135103041 5 prime UTR variant C/G;T snv 0.24 0.700 1.000 1 2016 2016
dbSNP: rs56131511
rs56131511
1 6 135068381 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs9402682
rs9402682
2 6 135085045 intron variant G/T snv 0.42 0.700 1.000 1 2016 2016