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: rs12552
rs12552
OLFM4
3 1.000 0.040 13 53051646 3 prime UTR variant A/G snv 0.58 0.700 1.000 4 2016 2019
dbSNP: rs2535629
rs2535629
ITIH3
9 0.827 0.040 3 52799203 intron variant G/A;C snv 0.820 1.000 4 2013 2019
dbSNP: rs10149470
rs10149470 		3 1.000 0.040 14 103551616 upstream gene variant A/G snv 0.54 0.700 1.000 3 2018 2019
dbSNP: rs12415800
rs12415800 		1 1.000 0.040 10 67864422 intergenic variant G/A;C snv 0.720 1.000 3 2018 2019
dbSNP: rs1021363
rs1021363
SORCS3
1 1.000 0.040 10 104851081 intron variant A/G snv 0.74 0.700 1.000 2 2018 2019
dbSNP: rs10774037
rs10774037
CACNA1C
3 0.882 0.040 12 2311360 intron variant G/A snv 0.77 0.800 1.000 2 2013 2019
dbSNP: rs11135349
rs11135349 		1 1.000 0.040 5 165096466 intron variant A/C snv 0.61 0.700 1.000 2 2018 2019
dbSNP: rs11599236
rs11599236
SORCS3
2 1.000 0.040 10 104694914 intron variant T/C;G snv 0.700 1.000 2 2018 2018
dbSNP: rs11663393
rs11663393
DCC
2 1.000 0.040 18 53088362 intron variant G/A snv 0.40 0.700 1.000 2 2018 2018
dbSNP: rs1226412
rs1226412
LINC01876
1 1.000 0.040 2 156254801 non coding transcript exon variant C/T snv 0.73 0.700 1.000 2 2018 2019
dbSNP: rs12520799
rs12520799
DCANP1 ; TIFAB
1 1.000 0.040 5 135446760 stop gained T/A;C snv 0.51 0.020 0.500 2 2011 2013
dbSNP: rs12967143
rs12967143
TCF4
1 1.000 0.040 18 55431781 intron variant G/C snv 0.55 0.700 1.000 2 2018 2019
dbSNP: rs12967855
rs12967855
CELF4
2 1.000 0.040 18 37558282 intron variant A/G snv 0.52 0.700 1.000 2 2018 2019
dbSNP: rs1354115
rs1354115
CARM1P1
1 1.000 0.040 9 2983774 intron variant C/A;T snv 0.700 1.000 2 2018 2019
dbSNP: rs1558477
rs1558477
LOC107986780
1 1.000 0.040 7 31115733 downstream gene variant T/C snv 0.56 0.800 1.000 2 2009 2011
dbSNP: rs1656369
rs1656369
LOC100996447
1 1.000 0.040 3 158562296 intron variant T/A snv 0.29 0.700 1.000 2 2016 2018
dbSNP: rs1806153
rs1806153
PAX6-AS1 ; PAUPAR
2 1.000 0.040 11 31828558 non coding transcript exon variant G/T snv 0.40 0.700 1.000 2 2018 2019
dbSNP: rs2715148
rs2715148
PCLO
1 1.000 0.040 7 82820719 3 prime UTR variant A/C snv 0.57 0.800 1.000 2 2009 2011
dbSNP: rs2876520
rs2876520 		1 1.000 0.040 6 142675481 intron variant C/A;G snv 0.53 0.700 1.000 2 2018 2019
dbSNP: rs35936514
rs35936514
LHPP
1 1.000 0.040 10 124556401 intron variant C/T snv 0.11 0.020 1.000 2 2016 2019
dbSNP: rs3793577
rs3793577
ELAVL2
1 1.000 0.040 9 23737629 intron variant A/C;G snv 0.700 1.000 2 2018 2019
dbSNP: rs3806843
rs3806843
PCDHA7 ; PCDHA6 ; PCDHA5 ; PCDHA4 ; PCDHA3 ; PCDHA2 ; PCDHA1
1 1.000 0.040 5 140832953 intron variant T/C snv 0.59 0.700 1.000 2 2016 2018
dbSNP: rs454214
rs454214
MEF2C-AS2
1 1.000 0.040 5 88707586 intron variant C/A;T snv 0.700 1.000 2 2016 2018
dbSNP: rs4543289
rs4543289
LOC105377703
1 1.000 0.040 5 165057942 non coding transcript exon variant T/G snv 0.57 0.700 1.000 2 2016 2018
dbSNP: rs4650608
rs4650608 		7 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 0.800 1.000 2 2013 2013