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: rs1420101
rs1420101
IL18R1 ; IL1RL1
8 0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35 0.800 1.000 1 2009 2009
dbSNP: rs2416257
rs2416257
WDR36
5 0.882 0.160 5 111099792 intron variant C/G;T snv 0.800 1.000 1 2009 2009
dbSNP: rs4143832
rs4143832 		4 0.925 0.080 5 132527285 intron variant T/G snv 0.76 0.800 1.000 1 2009 2009
dbSNP: rs4857855
rs4857855 		1 3 128541707 downstream gene variant C/T snv 0.18 0.800 1.000 1 2009 2009
dbSNP: rs10147992
rs10147992
STXBP6
3 14 25034593 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs10956483
rs10956483
CCDC26
3 8 129559864 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs11018874
rs11018874
NAALAD2
2 11 90142269 intron variant G/A snv 9.7E-02 0.700 1.000 1 2011 2011
dbSNP: rs12748961
rs12748961 		2 1 205707135 intergenic variant T/C snv 0.12 0.700 1.000 1 2011 2011
dbSNP: rs12988934
rs12988934
ITGA4
3 2 181458938 non coding transcript exon variant C/T snv 5.9E-02 0.700 1.000 1 2011 2011
dbSNP: rs2516399
rs2516399 		3 0.925 0.120 6 31513522 upstream gene variant A/G snv 0.11 0.800 1.000 1 2011 2011
dbSNP: rs3095254
rs3095254 		3 6 31253891 intergenic variant C/A;G snv 0.55 0.700 1.000 1 2011 2011
dbSNP: rs331615
rs331615 		1 20 57063481 intergenic variant T/A snv 0.44 0.800 1.000 1 2011 2011
dbSNP: rs4794822
rs4794822 		3 17 40000459 downstream gene variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs546829
rs546829 		2 4 74090655 upstream gene variant A/T snv 0.63 0.700 1.000 1 2011 2011
dbSNP: rs7237848
rs7237848 		2 18 4773111 downstream gene variant C/T snv 0.50 0.700 1.000 1 2011 2011
dbSNP: rs7275212
rs7275212
ERG
2 21 38480628 intron variant A/T snv 2.9E-02 0.700 1.000 1 2011 2011
dbSNP: rs7578982
rs7578982
ACOXL ; MIR4435-2HG
4 2 111078961 intron variant T/C snv 0.27 0.700 1.000 1 2011 2011
dbSNP: rs9373124
rs9373124
HBS1L
3 6 135102071 intron variant T/C snv 0.33 0.800 1.000 1 2011 2011
dbSNP: rs3184504
rs3184504
ATXN2 ; SH2B3
92 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.800 1.000 2 2009 2016
dbSNP: rs1000005
rs1000005
LINC00945
1 21 33060745 intron variant G/C snv 0.51 0.700 1.000 1 2016 2016
dbSNP: rs10045577
rs10045577
WDR36
1 5 111090753 intron variant C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10075801
rs10075801
SLC22A4 ; MIR3936HG
5 5 132341949 intron variant A/G snv 0.31 0.700 1.000 1 2016 2016
dbSNP: rs10138752
rs10138752
RAD51B
5 14 68713254 intron variant C/T snv 8.8E-02 0.700 1.000 1 2016 2016
dbSNP: rs10165200
rs10165200
LINC00299
2 2 8299499 intron variant G/A snv 0.36 0.700 1.000 1 2016 2016
dbSNP: rs10173538
rs10173538
BAZ2B ; MARCHF7
5 2 159712765 intron variant C/G;T snv 0.700 1.000 1 2016 2016