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: rs7635832
rs7635832
1 3 172271486 intron variant T/G snv 0.22 0.700 1.000 3 2017 2018
dbSNP: rs12492846
rs12492846
1 3 172208901 intron variant C/T snv 0.73 0.700 1.000 2 2018 2018
dbSNP: rs6445055
rs6445055
4 0.925 0.040 3 172274597 intron variant G/A snv 0.24 0.700 1.000 2 2014 2017
dbSNP: rs16856911
rs16856911
1 3 172082708 intron variant G/C snv 5.8E-02 0.700 1.000 1 2018 2018
dbSNP: rs4380442
rs4380442
1 3 172212591 intron variant G/A snv 0.90 0.700 1.000 1 2018 2018
dbSNP: rs62283814
rs62283814
1 3 172103766 intron variant C/T snv 0.18 0.700 1.000 1 2018 2018