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: rs10775354
rs10775354
RBFOX1
1 1.000 0.080 16 6757689 intron variant A/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs10780661
rs10780661
SLC28A3
1 1.000 0.080 9 84311392 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs1086603
rs1086603 		3 0.882 0.120 1 147816164 intergenic variant G/A snv 3.4E-02 0.700 1.000 1 2009 2009
dbSNP: rs10894993
rs10894993 		2 0.925 0.080 11 100627998 intergenic variant T/G snv 4.7E-02 0.700 1.000 1 2009 2009
dbSNP: rs10915020
rs10915020 		1 1.000 0.080 1 34692115 intergenic variant T/A snv 0.10 0.700 1.000 1 2013 2013
dbSNP: rs10918931
rs10918931 		1 1.000 0.080 1 168592853 intergenic variant T/C snv 0.61 0.700 1.000 1 2009 2009
dbSNP: rs10944489
rs10944489
MAP3K7
1 1.000 0.080 6 90554374 intron variant G/A snv 3.6E-02 0.700 1.000 1 2009 2009
dbSNP: rs10947261
rs10947261
BTNL2 ; TSBP1-AS1
4 0.882 0.240 6 32405455 splice region variant G/T snv 0.11 0.700 1.000 1 2009 2009
dbSNP: rs10956273
rs10956273
LINC00861
1 1.000 0.080 8 125953914 non coding transcript exon variant A/G snv 6.9E-02 0.700 1.000 1 2009 2009
dbSNP: rs10974284
rs10974284
GLIS3
1 1.000 0.080 9 4028700 intron variant T/C snv 1.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs11030600
rs11030600 		1 1.000 0.080 11 29174695 intron variant T/G snv 8.9E-02 0.700 1.000 1 2009 2009
dbSNP: rs1105358
rs1105358
C9orf92
1 1.000 0.080 9 16265821 intron variant G/C snv 0.10 0.700 1.000 1 2009 2009
dbSNP: rs11081843
rs11081843
NOL4
1 1.000 0.080 18 34103632 intron variant T/C snv 0.16 0.700 1.000 1 2009 2009
dbSNP: rs11083572
rs11083572
LOC100420587 ; LOC102724908
1 1.000 0.080 19 28604968 intron variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs11165851
rs11165851
DPYD ; LOC105378867
1 1.000 0.080 1 97380021 intron variant T/A snv 0.93 0.700 1.000 1 2009 2009
dbSNP: rs11189017
rs11189017 		1 1.000 0.080 10 81258621 intergenic variant T/G snv 1.0E-02 0.700 1.000 1 2009 2009
dbSNP: rs11206948
rs11206948
LOC105378745
1 1.000 0.080 1 56984813 intron variant T/C snv 3.6E-02 0.700 1.000 1 2009 2009
dbSNP: rs11210604
rs11210604 		2 0.925 0.080 1 42158001 downstream gene variant T/A;G snv 0.700 1.000 1 2009 2009
dbSNP: rs11221067
rs11221067 		1 1.000 0.080 11 127823799 intergenic variant C/T snv 8.8E-02 0.700 1.000 1 2009 2009
dbSNP: rs11238999
rs11238999
CXCL12
1 1.000 0.080 10 44345031 regulatory region variant G/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs11574049
rs11574049
VDR
1 1.000 0.080 12 47878732 intron variant A/G snv 1.6E-02 0.700 1.000 1 2009 2009
dbSNP: rs11603020
rs11603020
SERPING1
2 0.925 0.120 11 57606859 intron variant T/C snv 0.21 0.700 1.000 1 2009 2009
dbSNP: rs11604865
rs11604865
LRRC4C
1 1.000 0.080 11 40636452 intron variant T/C snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs1163521
rs1163521 		1 1.000 0.080 1 105786097 intergenic variant T/A;C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs11687856
rs11687856
GALNT14
1 1.000 0.080 2 31117780 intron variant G/A snv 0.19 0.700 1.000 1 2009 2009