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: rs11031006
rs11031006
LOC105376607
8 0.882 0.120 11 30204981 intron variant G/A snv 0.11 0.700 1.000 1 2015 2015
dbSNP: rs11070328
rs11070328
NUSAP1
1 15 41359371 intron variant T/C snv 0.21 0.700 1.000 1 2012 2012
dbSNP: rs11180609
rs11180609
LOC105369844
1 12 75646612 intron variant T/C snv 0.10 0.700 1.000 1 2019 2019
dbSNP: rs112241539
rs112241539
CASTOR3
1 7 100249614 intron variant C/T snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs11245450
rs11245450
ZRANB1
2 10 124969506 intron variant G/A snv 0.35 0.700 1.000 1 2019 2019
dbSNP: rs112869704
rs112869704
UQCRH
1 1 46314613 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs114158228
rs114158228
CDKAL1
1 6 20699892 intron variant T/A snv 4.2E-04 0.700 1.000 1 2013 2013
dbSNP: rs11586493
rs11586493
STX6
1 1 180992109 intron variant G/A snv 0.56 0.700 1.000 1 2019 2019
dbSNP: rs11738223
rs11738223
LOC105377727 ; LOC107984004
1 5 172507488 intron variant A/G snv 0.23 0.700 1.000 1 2015 2015
dbSNP: rs11786868
rs11786868
ZFHX4
1 8 76741709 intron variant C/A;G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs11935767
rs11935767
H2AZ1-DT
1 4 100093652 intron variant A/G snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs12132692
rs12132692
SELE ; C1orf112 ; LOC101928628
1 1 169763602 intron variant C/T snv 6.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs12142240
rs12142240
LRRC41
1 1 46281629 intron variant T/C snv 0.23 0.700 1.000 1 2015 2015
dbSNP: rs12211124
rs12211124
SYCP2L
1 6 10886352 intron variant T/C snv 0.31 0.700 1.000 1 2018 2018
dbSNP: rs12503643
rs12503643
ACSL1 ; LOC105377587
2 1.000 0.040 4 184824934 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs12599106
rs12599106 		1 16 35263654 intron variant T/A snv 0.36 0.700 1.000 1 2015 2015
dbSNP: rs13040088
rs13040088
DIDO1
1 20 62917850 intron variant A/G snv 0.19 0.700 1.000 1 2015 2015
dbSNP: rs13230316
rs13230316
NRCAM
1 7 108351123 intron variant C/G snv 0.29 0.700 1.000 1 2013 2013
dbSNP: rs13335395
rs13335395
TCF25
1 16 89886435 intron variant T/A snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs1411478
rs1411478
STX6
3 0.925 0.120 1 180993146 intron variant A/G snv 0.56 0.700 1.000 1 2015 2015
dbSNP: rs148727829
rs148727829
CCZ1
1 7 5910286 intron variant T/G snv 3.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs1551562
rs1551562
BRSK1
1 19 55303513 intron variant A/G snv 0.19 0.700 1.000 1 2009 2009
dbSNP: rs1635501
rs1635501
EXO1
1 1 241877473 intron variant C/T snv 0.54 0.800 1.000 1 2012 2012
dbSNP: rs1635506
rs1635506
EXO1
1 1 241865502 intron variant T/C snv 0.49 0.700 1.000 1 2019 2019
dbSNP: rs16858210
rs16858210
CYP2AB1P
1 3 183906222 intron variant G/A snv 0.31 0.700 1.000 1 2015 2015