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: rs7756992
rs7756992
12 0.827 0.240 6 20679478 intron variant A/G;T snv 0.060 1.000 6 2011 2017
dbSNP: rs10946398
rs10946398
7 0.827 0.160 6 20660803 intron variant A/C snv 0.40 0.020 1.000 2 2011 2019
dbSNP: rs7754840
rs7754840
9 0.807 0.200 6 20661019 intron variant G/A;C;T snv 0.020 1.000 2 2011 2016