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: rs9989419
rs9989419 		11 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 0.700 1.000 6 2008 2014
dbSNP: rs9987289
rs9987289
LOC157273
10 1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 0.700 1.000 2 2010 2013
dbSNP: rs998584
rs998584 		11 6 43790159 downstream gene variant C/A snv 0.41 0.700 1.000 1 2013 2013
dbSNP: rs9984764
rs9984764
APP
3 21 26125180 intron variant G/A snv 1.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs9979085
rs9979085
IL10RB ; IL10RB-DT
2 21 33267925 intron variant C/G snv 1.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs9971916
rs9971916
PDE3A
2 12 20535707 intron variant A/T snv 0.99 0.700 1.000 1 2012 2012
dbSNP: rs9943924
rs9943924
TNFSF11
2 13 42568548 intron variant G/A snv 5.0E-02 0.700 1.000 1 2012 2012
dbSNP: rs9939224
rs9939224
CETP
6 1.000 0.040 16 56968820 intron variant T/G snv 0.75 0.700 1.000 1 2012 2012
dbSNP: rs9930761
rs9930761
CETP
2 16 56973280 intron variant T/C snv 5.9E-02 7.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs9923854
rs9923854
CETP
3 16 56983090 intron variant T/G snv 0.10 0.700 1.000 1 2012 2012
dbSNP: rs9913813
rs9913813
LOC105371790
4 17 44277325 intron variant G/A snv 1.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs9913758
rs9913758
MYOCD ; LOC100128006
4 17 12763404 synonymous variant C/G;T snv 6.5E-03; 4.1E-06 2.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs9908890
rs9908890 		2 17 41710043 upstream gene variant A/G snv 3.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs9891572
rs9891572 		3 1.000 0.040 17 2525214 intergenic variant C/T snv 0.17 0.700 1.000 1 2009 2009
dbSNP: rs9836225
rs9836225
MGLL
3 3 127797551 intron variant C/T snv 7.4E-03 0.700 1.000 1 2012 2012
dbSNP: rs9826676
rs9826676
GNAI2
2 3 50243648 intron variant G/C snv 1.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs970548
rs970548
MARCHF8
3 10 45517829 intron variant A/C;T snv 0.700 1.000 1 2013 2013
dbSNP: rs9658292
rs9658292
NOS1
5 12 117318980 intron variant G/C snv 9.4E-04 0.700 1.000 1 2012 2012
dbSNP: rs9658113
rs9658113
PPARD
2 6 35397017 intron variant C/T snv 8.6E-04 0.700 1.000 1 2012 2012
dbSNP: rs9644636
rs9644636
LPL
3 8 19967385 downstream gene variant T/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs964184
rs964184
ZPR1
47 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.700 1.000 6 2009 2013
dbSNP: rs9622186
rs9622186 		6 22 35377961 upstream gene variant A/G snv 3.7E-03 0.700 1.000 1 2012 2012
dbSNP: rs956084
rs956084
FAF1
2 1 50445675 intron variant C/T snv 3.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs9556465
rs9556465
ABCC4
2 13 95205263 intron variant G/T snv 3.4E-03 0.700 1.000 1 2012 2012
dbSNP: rs9465848
rs9465848
CDKAL1
4 6 20635589 intron variant C/T snv 9.3E-03 0.700 1.000 1 2012 2012