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: rs3774427
rs3774427
4 3 53531601 intron variant C/G snv 0.11 0.700 1.000 2 2018 2018
dbSNP: rs9810888
rs9810888
3 3 53601568 intron variant T/G snv 0.51 0.700 1.000 2 2015 2018
dbSNP: rs3774447
rs3774447
2 3 53561685 intron variant T/C snv 2.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs3821843
rs3821843
3 3 53523985 intron variant G/A snv 0.72 0.700 1.000 1 2017 2017
dbSNP: rs9814480
rs9814480
4 3 53556438 intron variant C/T snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs9821489
rs9821489
1 3 53541701 intron variant G/A snv 0.16 0.700 1.000 1 2019 2019