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: rs6108787
rs6108787 		5 20 10986566 intron variant T/G snv 0.46 0.700 1.000 1 2018 2018
dbSNP: rs62434109
rs62434109
PLEKHG1
5 6 150654176 intron variant T/G snv 8.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs11024074
rs11024074
PLEKHA7
5 0.925 0.040 11 16895672 intron variant T/C snv 0.29 0.700 1.000 1 2009 2009
dbSNP: rs11867410
rs11867410
APOH
3 17 66231245 intron variant T/C snv 4.0E-02 0.700 1.000 1 2013 2013
dbSNP: rs13082711
rs13082711 		5 3 27496418 intergenic variant T/C snv 0.16 0.700 1.000 1 2011 2011
dbSNP: rs1330225
rs1330225 		3 1 106293321 intergenic variant T/C snv 0.38 0.700 1.000 1 2013 2013
dbSNP: rs17135875
rs17135875
FBXL13
3 7 102878584 intron variant T/C snv 0.24 0.700 1.000 1 2013 2013
dbSNP: rs3753584
rs3753584
CLCN6 ; MTHFR
10 0.827 0.080 1 11804529 5 prime UTR variant T/C snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs604723
rs604723
ARHGAP42
9 1.000 0.040 11 100739815 intron variant T/C snv 0.78 0.700 1.000 1 2018 2018
dbSNP: rs7497026
rs7497026 		2 15 74916208 downstream gene variant T/C snv 0.46 0.700 1.000 1 2018 2018
dbSNP: rs7622665
rs7622665
ULK4
3 1.000 0.160 3 41929251 intron variant T/C snv 0.67 0.700 1.000 1 2018 2018
dbSNP: rs3184504
rs3184504
ATXN2 ; SH2B3
92 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.700 1.000 3 2009 2013
dbSNP: rs198851
rs198851
H4C3
15 6 26104404 downstream gene variant T/A;C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs2013002
rs2013002 		5 12 111762346 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs419076
rs419076
MECOM
6 3 169383098 intron variant T/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs2306363
rs2306363
SIPA1
7 11 65638129 5 prime UTR variant G/T snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs4373814
rs4373814 		5 10 18131043 intergenic variant G/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs1350193
rs1350193
CSK
2 15 74791940 intron variant G/C snv 0.67 0.700 1.000 1 2018 2018
dbSNP: rs1801253
rs1801253
ADRB1
34 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.700 1.000 1 2018 2018
dbSNP: rs17035646
rs17035646
CASZ1
6 1 10736490 intron variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1980235
rs1980235
LOC107984543
2 12 89717005 intron variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs9815354
rs9815354
ULK4
4 0.925 0.160 3 41871159 intron variant G/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs633185
rs633185
ARHGAP42
10 0.925 0.080 11 100722807 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs7922049
rs7922049
CABCOCO1
3 10 61702607 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs10255839
rs10255839
EVX1
6 7 27249498 intron variant G/A snv 0.87 0.700 1.000 1 2018 2018