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: rs13387347
rs13387347
SPC25
1 2 168898336 intron variant T/C snv 0.49 0.700 1.000 2 2015 2018
dbSNP: rs3847554
rs3847554 		1 11 92935660 upstream gene variant C/T snv 0.56 0.700 1.000 2 2015 2019
dbSNP: rs6048216
rs6048216
LNCNEF
1 20 22600630 intron variant T/C snv 0.17 0.700 1.000 2 2015 2019
dbSNP: rs10246797
rs10246797
SUGCT
1 7 40304762 intron variant C/A;G snv 0.45 0.700 1.000 1 2009 2009
dbSNP: rs10259649
rs10259649
GCK ; LOC105375257
1 7 44180106 intron variant T/C snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs10276674
rs10276674
DGKB
1 7 14882382 intron variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs10497345
rs10497345
SPC25
1 2 168878291 intron variant G/C snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs10815355
rs10815355
KANK1
1 9 622523 intron variant G/T snv 6.0E-02 0.700 1.000 1 2015 2015
dbSNP: rs10849893
rs10849893
KDM2B
1 12 121500382 intron variant C/G snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs1120557
rs1120557 		1 14 62662722 regulatory region variant A/G snv 0.88 0.700 1.000 1 2009 2009
dbSNP: rs11571943
rs11571943
CDC5L
1 6 44403953 synonymous variant T/C snv 2.1E-02 2.9E-02 0.700 1.000 1 2009 2009
dbSNP: rs118084662
rs118084662
DHRS7B
1 17 21169976 intron variant A/G snv 3.3E-04 0.700 1.000 1 2019 2019
dbSNP: rs12280680
rs12280680
CREB3L1
1 11 46279171 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs12385797
rs12385797 		1 11 106465562 upstream gene variant C/A snv 6.4E-02 0.700 1.000 1 2009 2009
dbSNP: rs13427272
rs13427272
CTNNA2
1 2 80058810 intron variant G/A snv 5.4E-02 0.700 1.000 1 2009 2009
dbSNP: rs143399767
rs143399767 		1 9 93420421 downstream gene variant A/C snv 6.9E-03 0.700 1.000 1 2017 2017
dbSNP: rs16993414
rs16993414 		1 20 7327891 intergenic variant T/C snv 2.4E-02 0.700 1.000 1 2009 2009
dbSNP: rs17066694
rs17066694 		1 5 166334297 intergenic variant A/G snv 4.8E-02 0.700 1.000 1 2009 2009
dbSNP: rs17407594
rs17407594 		1 1 65704679 intron variant G/A;T snv 0.700 1.000 1 2014 2014
dbSNP: rs225675
rs225675
VTA1
1 6 142190999 intron variant A/G snv 0.40 0.700 1.000 1 2014 2014
dbSNP: rs234148
rs234148
LOC105370650
1 14 97688682 upstream gene variant T/C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs2722425
rs2722425
ZMAT4
1 8 40626720 intron variant T/C snv 0.78 0.800 1.000 1 2007 2007
dbSNP: rs339416
rs339416
DNAH5
1 5 13986417 regulatory region variant G/A snv 3.5E-02 0.700 1.000 1 2009 2009
dbSNP: rs34177044
rs34177044
SPC25
1 2 168897975 intron variant G/A snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs370189685
rs370189685
WDR4
1 21 42856322 intron variant G/C snv 9.1E-04 0.700 1.000 1 2017 2017