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: rs610932
rs610932
2 0.851 0.080 11 60171834 downstream gene variant T/G snv 0.57 0.840 1.000 1 2011 2017
dbSNP: rs7935829
rs7935829
1 1.000 0.080 11 60175342 intron variant A/G snv 0.33 0.800 1.000 1 2011 2019
dbSNP: rs7232
rs7232
4 1.000 0.080 11 60173126 missense variant T/A snv 0.31 0.27 0.720 1.000 1 2011 2019
dbSNP: rs583791
rs583791
1 1.000 0.080 11 60179779 missense variant C/T snv 0.59 0.57 0.710 1.000 1 2011 2014
dbSNP: rs12453
rs12453
1 1.000 0.080 11 60178272 synonymous variant T/C snv 0.35 0.32 0.700 1.000 1 2011 2011
dbSNP: rs17602572
rs17602572
1 1.000 0.080 11 60180901 non coding transcript exon variant C/G snv 0.32 0.700 1.000 1 2011 2011
dbSNP: rs2278867
rs2278867
1 1.000 0.080 11 60175636 intron variant A/T snv 0.35 0.30 0.700 1.000 1 2011 2011