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: rs121917739
rs121917739
4 0.882 0.080 15 40718818 missense variant G/A snv 3.7E-04 1.7E-03 0.710 1.000 8 2000 2015
dbSNP: rs1801320
rs1801320
15 0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12 0.020 1.000 2 2007 2011
dbSNP: rs1801321
rs1801321
8 0.790 0.160 15 40695367 5 prime UTR variant G/C;T snv 0.35 0.010 1.000 1 2017 2017
dbSNP: rs2412546
rs2412546
2 0.925 0.080 15 40714325 intron variant G/A snv 0.49 0.010 1.000 1 2009 2009
dbSNP: rs4417527
rs4417527
3 0.882 0.120 15 40729082 intron variant C/G snv 0.22 0.010 1.000 1 2009 2009