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: rs157935
rs157935
4 0.851 0.040 7 130900794 intron variant T/G snv 0.28 0.700 1.000 2 2014 2015
dbSNP: rs125124
rs125124
3 0.882 0.040 7 130899925 intron variant C/G snv 0.28 0.700 1.000 1 2019 2019