Source: ALL
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: rs543874
rs543874 		11 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 0.700 1.000 4 2010 2013
dbSNP: rs1514175
rs1514175
TNNI3K ; FPGT-TNNI3K ; LRRC53
4 1.000 0.080 1 74525960 intron variant A/G snv 0.48 0.700 1.000 3 2010 2013
dbSNP: rs2815752
rs2815752
LOC105378797
7 0.925 0.200 1 72346757 intron variant G/A snv 0.62 0.700 1.000 3 2009 2013
dbSNP: rs1555543
rs1555543 		3 1 96479241 intergenic variant A/C snv 0.55 0.700 1.000 2 2010 2013
dbSNP: rs2568958
rs2568958
LOC105378797
8 0.882 0.160 1 72299433 intron variant G/A;C snv 0.700 1.000 2 2009 2013
dbSNP: rs574367
rs574367 		3 1 177904075 intron variant G/T snv 0.16 0.700 1.000 2 2012 2014
dbSNP: rs10789336
rs10789336
LOC105378797
3 1 72372723 intron variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs10913469
rs10913469
SEC16B ; CRYZL2P-SEC16B
7 1.000 0.080 1 177944384 intron variant T/C snv 0.22 0.700 1.000 1 2009 2009
dbSNP: rs11161721
rs11161721
COL24A1
4 1 86022231 intron variant C/A snv 0.27 0.27 0.700 1.000 1 2017 2017
dbSNP: rs113313252
rs113313252
TNNI3K ; FPGT-TNNI3K ; LRRC53
2 1 74534327 intron variant -/T delins 0.700 1.000 1 2013 2013
dbSNP: rs113722913
rs113722913
LOC105371682
3 1 199950846 intergenic variant T/C snv 2.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs12142020
rs12142020
TNNI3K ; FPGT-TNNI3K ; LRRC53
2 1 74534327 intron variant A/T snv 0.50 0.700 1.000 1 2013 2013
dbSNP: rs17124318
rs17124318
LINC01739
3 1 63015059 intron variant C/A;G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs201167096
rs201167096
TNNI3K ; FPGT-TNNI3K ; LRRC53
2 1 74534327 intron variant -/T delins 0.700 1.000 1 2013 2013
dbSNP: rs2785980
rs2785980
LYPLAL1-AS1
3 1 219527177 intergenic variant T/C snv 0.28 0.700 1.000 1 2012 2012
dbSNP: rs3934834
rs3934834
LOC105378948 ; LOC112267874
3 1 1070426 downstream gene variant C/T snv 0.21 0.700 1.000 1 2010 2010
dbSNP: rs516636
rs516636 		3 1 177886382 intron variant C/A snv 0.17 0.700 1.000 1 2012 2012
dbSNP: rs591120
rs591120
SEC16B ; CRYZL2P-SEC16B
3 1 177933618 missense variant G/A;C snv 4.0E-06; 0.42 0.700 1.000 1 2013 2013
dbSNP: rs633715
rs633715 		7 1.000 0.080 1 177883445 intron variant T/C snv 0.17 0.700 1.000 1 2013 2013
dbSNP: rs6689335
rs6689335
LYPLAL1-AS1
3 1 219455340 intron variant T/C snv 0.31 0.700 1.000 1 2017 2017
dbSNP: rs2867125
rs2867125 		8 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 0.800 1.000 3 2010 2015
dbSNP: rs12463617
rs12463617 		4 1.000 0.080 2 629244 regulatory region variant A/C;T snv 0.700 1.000 2 2013 2014
dbSNP: rs2890652
rs2890652 		3 2 142202362 intergenic variant T/C snv 0.21 0.700 1.000 2 2010 2013
dbSNP: rs6545814
rs6545814
ADCY3
3 2 24908447 intron variant A/G snv 0.53 0.700 1.000 2 2012 2014
dbSNP: rs713586
rs713586 		5 0.925 0.160 2 24935139 intergenic variant T/C snv 0.58 0.700 1.000 2 2010 2013