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: rs11922502
rs11922502 		1 3 32183711 intergenic variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs1277311
rs1277311
IGFBP7
1 4 57036595 intron variant C/T snv 0.49 0.700 1.000 1 2011 2011
dbSNP: rs236316
rs236316
BCAR3
1 1 93579040 intron variant C/T snv 0.43 0.700 1.000 1 2011 2011
dbSNP: rs7627367
rs7627367
ULK4
1 3 41569737 intron variant T/G snv 0.56 0.700 1.000 1 2011 2011
dbSNP: rs1021261
rs1021261
LUZP2
1 11 24720211 intron variant G/T snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs10262915
rs10262915
COL1A2-AS1
1 7 94371161 intron variant T/C snv 0.17 0.800 1.000 1 2012 2012
dbSNP: rs10834449
rs10834449
LUZP2
1 11 24718258 intron variant G/A snv 0.56 0.800 1.000 1 2012 2012
dbSNP: rs10995170
rs10995170
ZNF365
1 10 62463624 intron variant T/C snv 0.30 0.800 1.000 1 2012 2012
dbSNP: rs11099040
rs11099040 		1 4 130210261 intergenic variant C/T snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs11102986
rs11102986
RXRA
1 9 134393657 intron variant A/G snv 0.86 0.700 1.000 1 2012 2012
dbSNP: rs11703808
rs11703808
PISD
1 22 31628994 intron variant A/G snv 0.49 0.800 1.000 1 2012 2012
dbSNP: rs11713158
rs11713158
CNTN4
1 3 2854000 intron variant T/C snv 0.79 0.800 1.000 1 2012 2012
dbSNP: rs12627933
rs12627933
PISD
1 22 31631463 intron variant G/A snv 0.20 0.700 1.000 1 2012 2012
dbSNP: rs12798374
rs12798374
LUZP2
1 11 24720113 intron variant C/T snv 9.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs13113376
rs13113376 		1 4 130211745 intergenic variant T/C snv 0.18 0.700 1.000 1 2012 2012
dbSNP: rs13221576
rs13221576
COL1A2-AS1
1 7 94377682 intron variant C/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs1329573
rs1329573
PAX5
1 9 36998996 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1550404
rs1550404
LOC105373602
1 2 126573377 intergenic variant T/G snv 5.1E-02 0.800 1.000 1 2012 2012
dbSNP: rs16835742
rs16835742
CSMD2
1 1 33715242 intron variant G/T snv 8.8E-02 0.800 1.000 1 2012 2012
dbSNP: rs17584516
rs17584516
CNTN4 ; LOC105376926
1 3 2844843 intron variant A/G snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs1908038
rs1908038 		1 4 130212336 intergenic variant C/T snv 0.86 0.700 1.000 1 2012 2012
dbSNP: rs1908039
rs1908039 		1 4 130206478 intergenic variant T/A;C snv 0.800 1.000 1 2012 2012
dbSNP: rs1987511
rs1987511 		1 10 5306374 upstream gene variant T/C snv 0.44 0.800 1.000 1 2012 2012
dbSNP: rs2303690
rs2303690
ELSPBP1
1 19 48022250 missense variant G/A;C snv 0.62 0.700 1.000 1 2012 2012
dbSNP: rs2348114
rs2348114
LINC01792 ; AOX3P ; AOX3P-AOX2P
1 2 200717470 non coding transcript exon variant T/C snv 0.82 0.700 1.000 1 2012 2012