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: rs10237735
rs10237735
PDE1C
2 7 32337136 intron variant C/T snv 7.6E-02 0.700 1.000 1 2013 2013
dbSNP: rs10414689
rs10414689 		2 19 51293045 regulatory region variant T/C snv 0.11 0.700 1.000 1 2013 2013
dbSNP: rs10498676
rs10498676
ELOVL2
3 0.925 0.040 6 11026766 intron variant G/A snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs10517480
rs10517480 		2 4 59883111 intergenic variant A/T snv 0.27 0.700 1.000 1 2008 2008
dbSNP: rs1058694
rs1058694
AGPAT3
1 21 43984239 3 prime UTR variant C/T snv 0.32 0.700 1.000 1 2011 2011
dbSNP: rs10792320
rs10792320 		1 11 61978819 intergenic variant A/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs10809457
rs10809457
LOC105375974
2 9 11402319 intron variant G/T snv 0.36 0.700 1.000 1 2013 2013
dbSNP: rs108499
rs108499
MYRF ; TMEM258
2 11 61779765 intron variant C/T snv 0.27 0.700 1.000 1 2011 2011
dbSNP: rs10897208
rs10897208 		1 11 62024415 intergenic variant A/T snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs1109748
rs1109748
BEST1 ; LOC107984334
2 11 61955173 synonymous variant C/A snv 0.21 0.11 0.700 1.000 1 2011 2011
dbSNP: rs11119805
rs11119805
LPGAT1
2 1 211744902 3 prime UTR variant T/A snv 0.13 0.700 1.000 1 2013 2013
dbSNP: rs11120822
rs11120822
CAMTA1
2 1 7053052 intron variant G/C snv 0.34 0.700 1.000 1 2013 2013
dbSNP: rs11190604
rs11190604
HIF1AN
2 10 100542700 intron variant A/G snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs11230815
rs11230815 		2 11 61868654 downstream gene variant G/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs11230874
rs11230874 		1 11 62028114 intergenic variant T/G snv 6.9E-02 0.700 1.000 1 2011 2011
dbSNP: rs1145652
rs1145652 		1 5 165337081 intergenic variant A/G snv 9.6E-02 0.700 1.000 1 2011 2011
dbSNP: rs11667159
rs11667159 		3 19 46291989 intergenic variant C/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs11668290
rs11668290 		3 19 46292921 upstream gene variant G/A snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs11671319
rs11671319 		3 19 46291810 intergenic variant T/C snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs11671360
rs11671360 		3 19 46291914 intergenic variant T/C snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs11671710
rs11671710 		3 19 46288677 regulatory region variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs116843064
rs116843064
ANGPTL4
16 0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 0.700 1.000 1 2017 2017
dbSNP: rs11730235
rs11730235
STIM2
1 4 26922822 intron variant G/T snv 0.26 0.700 1.000 1 2011 2011
dbSNP: rs117366905
rs117366905 		3 19 46294033 upstream gene variant A/G snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs117992292
rs117992292 		3 19 46294038 upstream gene variant A/G snv 0.12 0.700 1.000 1 2017 2017