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: rs4269383
rs4269383
LOC101928923 ; LOC105378072
3 0.882 0.120 6 155876368 intergenic variant A/G snv 0.37 0.700 1.000 1 2011 2011
dbSNP: rs4285214
rs4285214
ZNF608
1 1.000 0.120 5 124688588 intron variant T/G snv 0.55 0.700 1.000 1 2017 2017
dbSNP: rs450960
rs450960
MICAL3
1 1.000 0.120 22 17833538 intron variant C/T snv 0.30 0.700 1.000 1 2018 2018
dbSNP: rs4927850
rs4927850
TFRC
2 0.925 0.120 3 196024759 intron variant T/C snv 0.71 0.700 1.000 1 2011 2011
dbSNP: rs5768709
rs5768709
TAFA5
2 0.925 0.120 22 48533757 intron variant A/G snv 0.36 0.700 1.000 1 2011 2011
dbSNP: rs6073450
rs6073450
LINC01620
1 1.000 0.120 20 44458008 intron variant G/A snv 0.43 0.700 1.000 1 2015 2015
dbSNP: rs6464375
rs6464375
DPP6
2 0.925 0.120 7 153928758 intron variant C/T snv 6.7E-02 0.700 1.000 1 2010 2010
dbSNP: rs6537481
rs6537481 		1 1.000 0.120 4 147474942 intergenic variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs6662005
rs6662005
ERO1B
1 1.000 0.120 1 236276616 intron variant G/A snv 0.16 0.700 1.000 1 2017 2017
dbSNP: rs687289
rs687289
ABO
15 1.000 0.120 9 133261703 intron variant A/G snv 0.700 1.000 1 2014 2014
dbSNP: rs708224
rs708224
BICD1
2 0.925 0.120 12 32283475 intron variant A/G snv 0.50 0.700 1.000 1 2010 2010
dbSNP: rs7214041
rs7214041
LINC00511 ; LINC00673
1 1.000 0.120 17 72405335 intron variant C/T snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs7310409
rs7310409
HNF1A
7 0.925 0.160 12 120987058 intron variant A/C;G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs7330800
rs7330800 		1 1.000 0.120 13 63573938 intergenic variant A/C;T snv 0.700 1.000 1 2017 2017
dbSNP: rs73328514
rs73328514
TNS3
1 1.000 0.120 7 47448971 intron variant A/T snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs77038344
rs77038344
TNS4
1 1.000 0.120 17 40487962 intron variant C/T snv 8.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs7859034
rs7859034
SMC2
4 0.851 0.120 9 104103411 intron variant G/T snv 0.60 0.700 1.000 1 2019 2019
dbSNP: rs876493
rs876493
PNMT
2 0.925 0.160 17 39668292 intron variant G/A snv 0.47 0.700 1.000 1 2019 2019
dbSNP: rs9363918
rs9363918 		3 0.882 0.200 6 68432116 intron variant T/G snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs9502893
rs9502893 		5 0.827 0.120 6 1339954 intergenic variant C/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs9554197
rs9554197
PLUT ; LOC105370130
1 1.000 0.120 13 27902841 intron variant C/T snv 0.34 0.700 1.000 1 2015 2015
dbSNP: rs9573163
rs9573163 		2 0.925 0.120 13 73334709 regulatory region variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs962856
rs962856
LINC01829
1 1.000 0.120 2 67366671 intron variant C/T snv 0.66 0.700 1.000 1 2015 2015
dbSNP: rs981621
rs981621
LDLRAD4
1 1.000 0.120 18 13357201 intron variant A/C;G snv 0.40 0.700 1.000 1 2017 2017
dbSNP: rs104894360
rs104894360
KRAS
14 0.724 0.560 12 25209904 missense variant T/A;C snv 0.700 0