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: rs943580
rs943580 		2 1 230701298 upstream gene variant G/A snv 0.42 0.700 1.000 1 2011 2011
dbSNP: rs10197121
rs10197121
RRM2
1 2 10153562 intron variant C/T snv 0.64 0.700 1.000 1 2011 2011
dbSNP: rs13002573
rs13002573 		3 2 164058698 intron variant A/G snv 0.20 0.700 1.000 1 2011 2011
dbSNP: rs13424629
rs13424629
RRM2
1 2 10156359 intron variant T/C snv 0.15 0.700 1.000 1 2011 2011
dbSNP: rs1446468
rs1446468 		4 2 164106976 intron variant T/C snv 0.40 0.700 1.000 1 2011 2011
dbSNP: rs16849225
rs16849225 		5 2 164050310 intron variant C/T snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs2110641
rs2110641
RRM2
1 2 10151287 intron variant G/C snv 0.65 0.700 1.000 1 2011 2011
dbSNP: rs2241113
rs2241113
RRM2
1 2 10135619 intron variant A/C snv 0.59 0.700 1.000 1 2011 2011
dbSNP: rs4638749
rs4638749 		2 2 108267586 downstream gene variant G/A snv 0.26 0.700 1.000 1 2014 2014
dbSNP: rs5743185
rs5743185
PMS1 ; LOC105373796
1 2 189873112 intron variant G/A snv 6.0E-02 0.700 1.000 1 2011 2011
dbSNP: rs6749447
rs6749447
STK39
2 2 168184876 intron variant T/G snv 0.37 0.800 1.000 1 2009 2009
dbSNP: rs72864420
rs72864420 		1 2 146515745 intergenic variant G/A snv 3.3E-02 0.700 1.000 1 2011 2011
dbSNP: rs7591163
rs7591163 		2 2 227850659 intergenic variant C/A;G;T snv 0.700 1.000 1 2007 2007
dbSNP: rs780093
rs780093
GCKR
30 0.763 0.240 2 27519736 intron variant T/C snv 0.68 0.700 1.000 1 2011 2011
dbSNP: rs825937
rs825937 		1 2 4760437 intergenic variant C/A;T snv 0.700 1.000 1 2014 2014
dbSNP: rs13082711
rs13082711 		5 3 27496418 intergenic variant T/C snv 0.16 0.700 1.000 1 2011 2011
dbSNP: rs1343040
rs1343040
MECOM ; MECOM-AS1
1 3 169468505 intron variant G/A snv 0.36 0.700 1.000 1 2011 2011
dbSNP: rs16833934
rs16833934 		3 3 164019462 intergenic variant A/G snv 0.34 0.700 1.000 1 2014 2014
dbSNP: rs1687295
rs1687295
FGD5
1 3 14848249 intron variant T/C snv 0.76 0.700 1.000 1 2011 2011
dbSNP: rs1717027
rs1717027
ULK4
3 1.000 0.160 3 41946428 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs2293947
rs2293947
EEFSEC
2 1.000 0.040 3 128378653 intron variant A/C snv 8.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs319690
rs319690
MAP4
4 3 47885994 intron variant T/C snv 0.39 0.700 1.000 1 2011 2011
dbSNP: rs3773643
rs3773643
TGFBR2
2 3 30668751 intron variant A/G snv 0.19 0.700 1.000 1 2007 2007
dbSNP: rs3774372
rs3774372
ULK4
4 1.000 0.160 3 41835922 missense variant T/C snv 0.17 0.18 0.700 1.000 1 2011 2011
dbSNP: rs419076
rs419076
MECOM
6 3 169383098 intron variant T/A;C snv 0.700 1.000 1 2011 2011