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: rs6420094
rs6420094
5 1.000 0.080 5 177390635 intron variant A/G snv 0.29 0.800 1.000 2 2013 2016
dbSNP: rs3812036
rs3812036
5 0.925 0.120 5 177386403 intron variant C/T snv 0.23 0.20 0.700 1.000 4 2017 2019
dbSNP: rs12659266
rs12659266
1 5 177380196 intron variant C/T snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs33921462
rs33921462
1 5 177387655 intron variant G/A snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs35610898
rs35610898
1 5 177388765 intron variant G/C snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs35716097
rs35716097
3 5 177379635 intron variant C/T snv 0.34 0.700 1.000 1 2016 2016
dbSNP: rs3812035
rs3812035
4 1.000 0.040 5 177390142 3 prime UTR variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs6862195
rs6862195
2 5 177395511 intron variant G/T snv 0.29 0.700 1.000 1 2019 2019