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: rs10180496
rs10180496 		1 1.000 0.040 2 12828774 intron variant A/G snv 0.15 0.800 1.000 1 2013 2013
dbSNP: rs10242311
rs10242311
ATXN7L1
1 1.000 0.040 7 105633273 intron variant A/C snv 6.2E-02 0.800 1.000 1 2013 2013
dbSNP: rs11166135
rs11166135 		1 1.000 0.040 1 98883280 intergenic variant A/G snv 0.10 0.800 1.000 1 2013 2013
dbSNP: rs12602978
rs12602978 		1 1.000 0.040 17 27240054 intron variant C/T snv 9.3E-02 0.800 1.000 1 2013 2013
dbSNP: rs1383934
rs1383934
ADAMTS3
1 1.000 0.040 4 72551807 intron variant G/A snv 0.68 0.800 1.000 1 2012 2012
dbSNP: rs1429138
rs1429138 		1 1.000 0.040 4 147361190 regulatory region variant T/A;C snv 0.800 1.000 1 2013 2013
dbSNP: rs17057381
rs17057381
EPHX2
1 1.000 0.040 8 27559284 upstream gene variant G/A snv 4.8E-02 0.800 1.000 1 2012 2012
dbSNP: rs2531154
rs2531154
PROM1
1 1.000 0.040 4 16016701 intron variant C/T snv 0.89 0.800 1.000 1 2013 2013
dbSNP: rs3114018
rs3114018
ABCG2
4 0.882 0.160 4 88143429 intron variant A/C snv 0.48 0.800 1.000 1 2013 2013
dbSNP: rs3896439
rs3896439
LOC107985376
1 1.000 0.040 1 4608610 intergenic variant G/A snv 9.4E-02 0.800 1.000 1 2013 2013
dbSNP: rs399593
rs399593
LYZL2
1 1.000 0.040 10 30623101 intron variant G/T snv 0.86 0.800 1.000 1 2013 2013
dbSNP: rs4251631
rs4251631
CDKN3
1 1.000 0.040 14 54409466 intron variant T/C snv 0.28 0.800 1.000 1 2012 2012
dbSNP: rs635808
rs635808
RPS6KA2
1 1.000 0.040 6 166763934 intron variant G/A snv 0.27 0.800 1.000 1 2012 2012
dbSNP: rs9308447
rs9308447 		1 1.000 0.040 1 9372331 downstream gene variant C/T snv 0.27 0.800 1.000 1 2013 2013
dbSNP: rs931608
rs931608
ZNF98
2 1.000 0.040 19 22431320 intron variant A/C;T snv 0.800 1.000 1 2013 2013
dbSNP: rs9793739
rs9793739
LINC02815 ; LINC02814
1 1.000 0.040 1 229150111 intron variant G/A snv 9.6E-02 0.800 1.000 1 2012 2012
dbSNP: rs10048146
rs10048146 		3 1.000 0.040 16 86677054 regulatory region variant A/G snv 0.17 0.700 1.000 1 2019 2019
dbSNP: rs10772314
rs10772314
LINC02446 ; LOC105369658
1 1.000 0.040 12 10551751 upstream gene variant T/A snv 0.47 0.700 1.000 1 2019 2019
dbSNP: rs10811723
rs10811723 		1 1.000 0.040 9 22542286 intergenic variant A/G snv 0.55 0.700 1.000 1 2019 2019
dbSNP: rs10851907
rs10851907
CHRNB4
4 1.000 0.040 15 78623522 upstream gene variant G/A snv 0.40 0.700 1.000 1 2019 2019
dbSNP: rs10987008
rs10987008
PBX3
1 1.000 0.040 9 125899321 intron variant T/A snv 0.54 0.700 1.000 1 2019 2019
dbSNP: rs1108343
rs1108343 		1 1.000 0.040 16 51177684 non coding transcript exon variant T/C snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs1122171
rs1122171
C5orf66
1 1.000 0.040 5 135174297 intron variant C/T snv 0.56 0.700 1.000 1 2019 2019
dbSNP: rs11672900
rs11672900
MAMSTR
1 1.000 0.040 19 48717066 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11676272
rs11676272
ADCY3
5 1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57 0.700 1.000 1 2019 2019