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: rs11216230
rs11216230
SIK3
2 11 117014073 intron variant G/A snv 3.1E-02 0.700 1.000 1 2014 2014
dbSNP: rs12594733
rs12594733
RORA
2 15 60952685 intron variant T/C snv 0.25 0.700 1.000 1 2014 2014
dbSNP: rs78557978
rs78557978 		2 4 114717445 upstream gene variant G/A;C snv 0.700 1.000 1 2014 2014
dbSNP: rs10019888
rs10019888 		3 4 26061368 regulatory region variant A/G snv 0.17 0.700 1.000 1 2013 2013
dbSNP: rs1047891
rs1047891
CPS1
34 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 0.700 1.000 1 2013 2013
dbSNP: rs1077835
rs1077835
LIPC ; ALDH1A2
5 15 58431227 intron variant A/G snv 0.34 0.700 1.000 1 2013 2013
dbSNP: rs10818782
rs10818782
GABBR2
2 9 98325004 intron variant G/A snv 0.60 0.700 1.000 1 2013 2013
dbSNP: rs11217785
rs11217785
POU2F3 ; LOC105369531
2 11 120281882 intron variant C/T snv 0.33 0.700 1.000 1 2013 2013
dbSNP: rs1121980
rs1121980
FTO
18 0.807 0.240 16 53775335 intron variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs11246602
rs11246602 		2 11 54607190 upstream gene variant A/G snv 0.11 0.700 1.000 1 2013 2013
dbSNP: rs12145743
rs12145743
RRNAD1
4 1 156730859 intron variant T/G snv 0.24 0.700 1.000 1 2013 2013
dbSNP: rs12748152
rs12748152 		8 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 0.700 1.000 1 2013 2013
dbSNP: rs12801636
rs12801636
PCNX3
5 1.000 0.040 11 65623846 intron variant G/A snv 0.25 0.700 1.000 1 2013 2013
dbSNP: rs12979813
rs12979813
DOCK6
4 19 11232027 intron variant A/G snv 0.30 0.700 1.000 1 2013 2013
dbSNP: rs13326165
rs13326165
STAB1
3 3 52498102 intron variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1461729
rs1461729
LOC157273
5 1.000 8 9329732 intron variant A/G snv 0.88 0.700 1.000 1 2013 2013
dbSNP: rs17173637
rs17173637
AOC1 ; LOC105375567
2 7 150832361 intron variant T/C snv 8.2E-02 0.700 1.000 1 2013 2013
dbSNP: rs17404153
rs17404153
DNAJC13
5 3 132444356 intron variant G/T snv 0.10 0.700 1.000 1 2013 2013
dbSNP: rs17695224
rs17695224
FPR3 ; ZNF577
2 19 51820963 intron variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs1936800
rs1936800 		4 6 127114919 intron variant C/T snv 0.51 0.700 1.000 1 2013 2013
dbSNP: rs2013208
rs2013208
RBM6 ; RBM5
4 3 50091966 intron variant C/T snv 0.61 0.56 0.700 1.000 1 2013 2013
dbSNP: rs2126259
rs2126259
LOC157273
9 1.000 8 9327636 intron variant T/C snv 0.87 0.700 1.000 1 2013 2013
dbSNP: rs2278426
rs2278426
ANGPTL8 ; DOCK6
11 1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 0.700 1.000 1 2013 2013
dbSNP: rs2290547
rs2290547
SETD2
2 3 47019693 intron variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs2366858
rs2366858 		2 7 80711306 regulatory region variant C/A snv 0.94 0.700 1.000 1 2013 2013