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: rs11705729
rs11705729
IGF2BP2
3 1.000 0.080 3 185789511 intron variant A/T snv 0.45 0.700 1.000 1 2018 2018
dbSNP: rs11924032
rs11924032
SLC2A2
3 3 171017310 intron variant G/A snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs7632505
rs7632505
SEMA5B
17 0.827 0.120 3 123019460 intron variant A/G snv 0.34 0.700 1.000 1 2016 2016
dbSNP: rs13114738
rs13114738
SLC39A8
16 0.851 0.120 4 102363708 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1869717
rs1869717
MAML3
16 0.851 0.120 4 139829967 intron variant G/C snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs2087160
rs2087160
ENPEP
2 4 110413574 intron variant G/T snv 0.68 0.700 1.000 1 2011 2011
dbSNP: rs4253252
rs4253252
KLKB1
3 4 186236304 intron variant T/G snv 0.56 0.700 1.000 1 2011 2011
dbSNP: rs4481233
rs4481233
SLC2A9
5 0.925 0.120 4 9954455 intron variant C/T snv 0.16 0.700 1.000 1 2011 2011
dbSNP: rs6533530
rs6533530 		16 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 0.700 1.000 1 2016 2016
dbSNP: rs8396
rs8396
ETFDH ; PPID
4 4 158709665 3 prime UTR variant T/C snv 0.29 0.700 1.000 1 2011 2011
dbSNP: rs272889
rs272889
SLC22A4 ; MIR3936HG
2 5 132329685 intron variant A/G snv 0.64 0.700 1.000 1 2011 2011
dbSNP: rs4704221
rs4704221
CERT1
16 0.851 0.120 5 75463358 intron variant T/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs5744680
rs5744680
POLK
18 0.851 0.120 5 75584065 intron variant G/A snv 0.55 0.700 1.000 1 2016 2016
dbSNP: rs7703051
rs7703051 		18 0.851 0.120 5 75329662 intron variant C/A snv 0.38 0.700 1.000 1 2016 2016
dbSNP: rs9942416
rs9942416 		9 5 75741470 intergenic variant C/G snv 0.53 0.700 1.000 1 2016 2016
dbSNP: rs3765467
rs3765467
GLP1R
3 1.000 0.080 6 39065819 missense variant G/A;C;T snv 3.6E-02 1.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs494562
rs494562 		2 6 85407411 intergenic variant A/G snv 0.16 0.700 1.000 1 2011 2011
dbSNP: rs662138
rs662138
SLC22A1
2 6 160143444 intron variant C/G snv 0.14 0.700 1.000 1 2011 2011
dbSNP: rs7760535
rs7760535
REV3L ; MFSD4B
3 6 111425880 intron variant G/C snv 0.46 0.700 1.000 1 2011 2011
dbSNP: rs9358356
rs9358356
CDKAL1
3 1.000 0.080 6 20667151 intron variant T/C snv 0.39 0.700 1.000 1 2018 2018
dbSNP: rs9393903
rs9393903
ELOVL2 ; ELOVL2-AS1
3 6 11042676 intron variant G/A snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs10244051
rs10244051 		3 1.000 0.080 7 15024208 intergenic variant T/A;G snv 0.800 1.000 1 2009 2009
dbSNP: rs12670403
rs12670403
AHR ; LOC101927609
2 7 17269655 intron variant C/A snv 0.46 0.700 1.000 1 2011 2011
dbSNP: rs1558318
rs1558318 		3 1.000 0.080 7 15025987 intergenic variant A/T snv 0.55 0.700 1.000 1 2018 2018
dbSNP: rs17140821
rs17140821 		16 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 0.700 1.000 1 2016 2016