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: rs17577094
rs17577094
3 0.925 0.120 17 46110126 intron variant A/G snv 0.14 0.800 1.000 1 2014 2014
dbSNP: rs2668692
rs2668692
3 1.000 0.040 17 46215654 intron variant G/A;T snv 0.700 1.000 3 2009 2012
dbSNP: rs546433642
rs546433642
4 0.925 0.120 17 46172742 intron variant T/C;G snv 0.700 1.000 3 2009 2012
dbSNP: rs549599956
rs549599956
4 0.925 0.120 17 46169798 intron variant A/G snv 0.700 1.000 3 2009 2012
dbSNP: rs7225002
rs7225002
7 0.925 0.080 17 46111701 intron variant A/G snv 0.39 0.700 1.000 3 2009 2012
dbSNP: rs17574228
rs17574228
3 0.925 0.120 17 46027143 3 prime UTR variant T/C snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17574361
rs17574361
2 1.000 0.040 17 46030836 3 prime UTR variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17574604
rs17574604
3 0.925 0.120 17 46034247 synonymous variant A/G snv 0.15 0.14 0.700 1.000 1 2012 2012
dbSNP: rs544161107
rs544161107
2 1.000 0.040 17 46144969 intron variant G/A snv 0.700 1.000 1 2011 2011
dbSNP: rs541455835
rs541455835
1 1.000 0.040 17 46099939 intron variant A/- del 0.14 0.010 1.000 1 2018 2018
dbSNP: rs7521
rs7521
3 0.925 0.080 17 46028029 3 prime UTR variant A/C;G snv 0.010 1.000 1 2009 2009