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: rs9854771
rs9854771
TP63
2 0.925 0.240 3 189790682 intron variant G/A snv 0.34 0.700 1.000 2 2015 2018
dbSNP: rs10500715
rs10500715
SBF2
2 0.925 0.120 11 9951515 intron variant T/G snv 0.39 0.700 1.000 1 2014 2014
dbSNP: rs10835188
rs10835188
LIN7C
2 1.000 0.120 11 27501639 intron variant G/T snv 0.68 0.700 1.000 1 2017 2017
dbSNP: rs10919791
rs10919791 		2 0.925 0.240 1 199996040 intergenic variant G/A snv 0.22 0.700 1.000 1 2014 2014
dbSNP: rs10983614
rs10983614
ASTN2
1 1.000 0.120 9 117306874 intron variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs1169296
rs1169296
HNF1A
1 1.000 0.120 12 120990604 intron variant A/G snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs1182933
rs1182933
C12orf43
3 1.000 0.120 12 121016819 upstream gene variant C/T snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs12362504
rs12362504
SBF2 ; LOC101928008
2 0.925 0.120 11 9907995 intron variant T/C snv 0.37 0.700 1.000 1 2017 2017
dbSNP: rs12413624
rs12413624 		5 0.851 0.120 10 118519432 intergenic variant T/A snv 0.34 0.700 1.000 1 2011 2011
dbSNP: rs12456874
rs12456874
LDLRAD4
2 0.925 0.120 18 13366863 intron variant A/G snv 0.20 0.700 1.000 1 2014 2014
dbSNP: rs12478462
rs12478462 		1 1.000 0.120 2 152798206 intergenic variant T/G snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs12620038
rs12620038
EPCAM-DT
1 1.000 0.120 2 47248996 intron variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs12951345
rs12951345
HNF1B ; LOC105371754
1 1.000 0.120 17 37717865 intron variant C/A snv 0.80 0.700 1.000 1 2019 2019
dbSNP: rs1326889
rs1326889
LOC105373166
1 1.000 0.120 1 230727252 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1547374
rs1547374
LOC105372815
2 0.925 0.120 21 42358786 downstream gene variant A/G snv 0.32 0.700 1.000 1 2011 2011
dbSNP: rs16861827
rs16861827
IGSF21
1 1.000 0.120 1 18351676 intron variant C/T snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs17275283
rs17275283 		1 1.000 0.120 11 96970814 intron variant T/C snv 0.26 0.700 1.000 1 2017 2017
dbSNP: rs1944788
rs1944788 		1 1.000 0.120 11 96947703 intron variant T/C snv 0.27 0.700 1.000 1 2017 2017
dbSNP: rs2218400
rs2218400 		1 1.000 0.120 13 63564941 intergenic variant C/A snv 0.34 0.700 1.000 1 2017 2017
dbSNP: rs2255280
rs2255280
C9 ; DAB2
2 0.925 0.120 5 39394887 intron variant C/A snv 0.98 0.700 1.000 1 2011 2011
dbSNP: rs2417487
rs2417487
SMC2
1 1.000 0.120 9 104125300 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs31490
rs31490
CLPTM1L
8 0.776 0.280 5 1344343 splice region variant G/A;T snv 0.37; 8.0E-06 0.700 1.000 1 2014 2014
dbSNP: rs351365
rs351365
WNT2B
1 1.000 0.120 1 112503773 intron variant T/C;G snv 0.700 1.000 1 2015 2015
dbSNP: rs361052
rs361052
IQSEC1
1 1.000 0.120 3 13029299 intron variant A/G snv 0.73 0.700 1.000 1 2017 2017
dbSNP: rs372883
rs372883
BACH1
5 0.827 0.360 21 29345416 3 prime UTR variant T/C snv 0.53 0.700 1.000 1 2011 2011