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: rs894160
rs894160
4 0.882 0.120 15 89668592 intron variant C/T snv 0.29 0.020 1.000 2 2008 2013
dbSNP: rs1052700
rs1052700
3 1.000 0.040 15 89665079 3 prime UTR variant A/T snv 0.26 0.010 1.000 1 2013 2013
dbSNP: rs2304796
rs2304796
2 1.000 0.040 15 89667026 synonymous variant G/A;C snv 0.28; 1.2E-05 0.010 1.000 1 2013 2013