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: rs6544619
rs6544619
LOC112268413
1 2 42957589 intergenic variant C/T snv 0.52 0.700 1.000 1 2009 2009
dbSNP: rs10275663
rs10275663
GRB10
2 7 50729988 intron variant G/A snv 9.4E-02 0.700 1.000 1 2015 2015
dbSNP: rs10743353
rs10743353
LINC02398
2 12 20047028 intron variant C/T snv 0.60 0.700 1.000 1 2018 2018
dbSNP: rs1275986
rs1275986 		2 2 26689211 upstream gene variant C/A snv 0.50 0.700 1.000 1 2018 2018
dbSNP: rs13067306
rs13067306 		2 3 94524869 regulatory region variant G/A snv 0.17 0.700 1.000 1 2013 2013
dbSNP: rs13306556
rs13306556
MTHFR
2 1 11792053 intron variant C/T snv 0.10 0.700 1.000 1 2018 2018
dbSNP: rs1350193
rs1350193
CSK
2 15 74791940 intron variant G/C snv 0.67 0.700 1.000 1 2018 2018
dbSNP: rs148514273
rs148514273
SETD7
2 4 139543924 intron variant G/A snv 2.4E-02 0.700 1.000 1 2017 2017
dbSNP: rs1579381
rs1579381 		2 12 115118002 intergenic variant C/G snv 0.18 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: rs2030114
rs2030114
HNRNPA1P48
2 16 51576036 intron variant G/A snv 0.23 0.700 1.000 1 2013 2013
dbSNP: rs3792765
rs3792765
NPR3
2 5 32713730 intron variant A/G snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs7286472
rs7286472 		2 22 33990484 intergenic variant A/G snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs73306888
rs73306888
ZNF831
2 20 59173534 intron variant G/A snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs73437358
rs73437358
ATP2B1
2 12 89678299 intron variant G/A snv 0.15 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: rs79211428
rs79211428
ULK4
2 3 41880318 intron variant C/T snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs8029440
rs8029440 		2 15 90866284 upstream gene variant G/A snv 0.32 0.700 1.000 1 2018 2018
dbSNP: rs10504249
rs10504249
LINC01602 ; LOC105375856
3 8 57876522 intron variant A/G snv 1.7E-02 0.700 1.000 1 2013 2013
dbSNP: rs10930597
rs10930597 		3 2 173462117 intergenic variant C/T snv 0.14 0.700 1.000 1 2013 2013
dbSNP: rs11867410
rs11867410
APOH
3 17 66231245 intron variant T/C snv 4.0E-02 0.700 1.000 1 2013 2013
dbSNP: rs11887188
rs11887188 		3 2 234394166 intergenic variant C/T snv 0.11 0.700 1.000 1 2013 2013
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: rs1918974
rs1918974
MECOM ; MECOM-AS1
3 1.000 0.040 3 169448100 intron variant C/T snv 0.57 0.700 1.000 1 2009 2009