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: rs603424
rs603424
PKD2L1
13 1.000 0.080 10 100315722 intron variant G/A snv 0.34 0.800 1.000 2 2012 2013
dbSNP: rs780093
rs780093
GCKR
30 0.763 0.240 2 27519736 intron variant T/C snv 0.68 0.700 1.000 2 2011 2013
dbSNP: rs1000778
rs1000778
FADS3
3 1.000 0.040 11 61887833 intron variant A/G snv 0.59 0.700 1.000 1 2011 2011
dbSNP: rs1007323
rs1007323
SYCP2L ; LOC101928191
1 6 10953011 intron variant T/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs10237735
rs10237735
PDE1C
2 7 32337136 intron variant C/T snv 7.6E-02 0.700 1.000 1 2013 2013
dbSNP: rs10468017
rs10468017
ALDH1A2
12 0.851 0.120 15 58386313 intron variant C/T snv 0.24 0.800 1.000 1 2012 2012
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: rs10769780
rs10769780
SYT9
1 11 7345864 intron variant T/C snv 0.25 0.800 1.000 1 2012 2012
dbSNP: rs1077989
rs1077989
GPHN ; TMEM229B
3 1.000 0.080 14 67509105 intron variant A/C snv 0.39 0.800 1.000 1 2012 2012
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: 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: rs11662721
rs11662721
ABHD3
1 18 21681452 intron variant C/T snv 0.15 0.800 1.000 1 2012 2012
dbSNP: rs11730235
rs11730235
STIM2
1 4 26922822 intron variant G/T snv 0.26 0.700 1.000 1 2011 2011
dbSNP: rs12190237
rs12190237
SYCP2L
1 6 10922405 intron variant G/A snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs12199131
rs12199131
SYCP2L ; LOC101928191
1 6 10932336 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs12200867
rs12200867
SYCP2L ; LOC101928191
1 6 10939591 intron variant C/G snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs12207488
rs12207488
SYCP2L ; LOC101928191
1 6 10952103 intron variant G/A snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs12213249
rs12213249
SYCP2L
1 6 10926709 intron variant C/T snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs12214825
rs12214825
SYCP2L ; LOC101928191
1 6 10933145 intron variant C/T snv 0.20 0.700 1.000 1 2011 2011
dbSNP: rs1225717
rs1225717
SYCP2L
1 6 10978007 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs1225736
rs1225736
SYCP2L ; LOC101928191
1 6 10939156 intron variant A/G snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs1225741
rs1225741
SYCP2L ; LOC101928191
1 6 10952010 intron variant G/A snv 0.39 0.700 1.000 1 2011 2011
dbSNP: rs1225744
rs1225744
SYCP2L ; LOC101928191
1 6 10954307 intron variant C/T snv 0.35 0.700 1.000 1 2011 2011