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: rs10028805
rs10028805
BANK1
3 0.882 0.160 4 101816093 intron variant G/A snv 0.45 0.700 1.000 1 2016 2016
dbSNP: rs71597109
rs71597109
BANK1
2 0.925 0.120 4 101819845 intron variant C/T snv 0.27 0.700 1.000 1 2017 2017
dbSNP: rs2511713
rs2511713 		2 0.925 0.120 8 102565637 downstream gene variant A/G snv 0.25 0.700 1.000 1 2017 2017
dbSNP: rs2511714
rs2511714 		2 0.925 0.120 8 102566646 regulatory region variant T/G snv 0.41 0.700 1.000 2 2013 2016
dbSNP: rs898518
rs898518
LEF1
2 0.925 0.120 4 108095668 intron variant C/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs7690934
rs7690934
LEF1
2 0.925 0.120 4 108104709 intron variant T/C snv 0.57 0.700 1.000 1 2017 2017
dbSNP: rs2003869
rs2003869
LEF1
2 0.925 0.120 4 108105258 intron variant A/C;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs13401811
rs13401811
ACOXL
2 0.925 0.120 2 110858527 intron variant G/A snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs17483466
rs17483466
ACOXL ; MIR4435-2HG
5 0.827 0.280 2 111039881 intron variant A/G snv 0.15 0.700 1.000 3 2008 2013
dbSNP: rs58055674
rs58055674
ACOXL ; MIR4435-2HG
2 0.925 0.120 2 111074216 intron variant T/C snv 0.13 0.700 1.000 2 2016 2017
dbSNP: rs12711846
rs12711846
ACOXL ; ACOXL-AS1 ; MIR4435-2HG
4 0.851 0.160 2 111098716 non coding transcript exon variant A/G snv 0.26 0.700 1.000 1 2017 2017
dbSNP: rs1439287
rs1439287
ACOXL ; ACOXL-AS1 ; MIR4435-2HG
2 0.925 0.120 2 111114320 non coding transcript exon variant G/A snv 0.42 0.700 1.000 1 2014 2014
dbSNP: rs9308731
rs9308731
BCL2L11 ; MIR4435-2HG
2 0.925 0.120 2 111150685 intron variant G/A snv 0.59 0.700 1.000 1 2016 2016
dbSNP: rs6489882
rs6489882
OAS3
2 0.925 0.120 12 112943571 intron variant G/A snv 0.75 0.700 1.000 1 2017 2017
dbSNP: rs61904987
rs61904987
LOC107984390
2 0.925 0.120 11 113646481 intergenic variant C/A;G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs6858698
rs6858698
CAMK2D
2 0.925 0.120 4 113762688 upstream gene variant G/C snv 0.20 0.700 1.000 1 2014 2014
dbSNP: rs1476569
rs1476569 		2 0.925 0.120 4 113777540 intergenic variant A/G snv 0.34 0.700 1.000 1 2017 2017
dbSNP: rs35923643
rs35923643
GRAMD1B
3 0.925 0.120 11 123484683 intron variant A/G snv 0.15 0.700 1.000 2 2016 2017
dbSNP: rs735665
rs735665
GRAMD1B
8 0.776 0.280 11 123490689 intron variant G/A snv 0.15 0.700 1.000 4 2008 2014
dbSNP: rs2953196
rs2953196
GRAMD1B
2 0.925 0.120 11 123497625 intron variant A/G snv 0.81 0.700 1.000 1 2016 2016
dbSNP: rs4525246
rs4525246
GRAMD1B
4 0.851 0.160 11 123524538 intron variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs2267708
rs2267708
GPR37
2 0.925 0.120 7 124752458 intron variant C/T snv 0.47 0.700 1.000 1 2017 2017
dbSNP: rs17246404
rs17246404
POT1
2 0.925 0.120 7 124822607 3 prime UTR variant C/A;T snv 0.700 1.000 1 2014 2014
dbSNP: rs140099016
rs140099016
PCAT1 ; CASC19
2 0.925 0.120 8 127183089 intron variant T/C snv 0.700 1.000 1 2016 2016
dbSNP: rs2466029
rs2466029
PCAT1 ; CASC19
2 0.925 0.120 8 127188726 non coding transcript exon variant C/G;T snv 0.700 1.000 1 2017 2017