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: rs79246196
rs79246196
STAG3
4 0.925 0.080 7 100185286 intron variant C/T snv 1.8E-02 0.700 1.000 1 2017 2017
dbSNP: rs57083693
rs57083693
UTP20
3 1.000 0.080 12 101348402 intron variant T/C snv 0.23 0.700 1.000 1 2014 2014
dbSNP: rs12544026
rs12544026
NCALD
4 0.925 0.080 8 101819970 intron variant G/A snv 0.85 0.700 1.000 1 2017 2017
dbSNP: rs13107325
rs13107325
SLC39A8
34 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs115357105
rs115357105 		4 0.925 0.080 9 104376689 intergenic variant A/G snv 1.5E-02 0.700 1.000 1 2017 2017
dbSNP: rs61776290
rs61776290 		3 1.000 0.080 1 10634850 upstream gene variant C/T snv 8.7E-02 0.700 1.000 1 2014 2014
dbSNP: rs7906104
rs7906104
LINC02661
3 1.000 0.080 10 108737343 intron variant C/T snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs17125651
rs17125651 		3 1.000 0.080 10 109063325 intergenic variant T/C snv 0.14 0.700 1.000 1 2019 2019
dbSNP: rs11066001
rs11066001
BRAP
15 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 0.700 1.000 1 2019 2019
dbSNP: rs671
rs671
ALDH2
116 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.700 1.000 1 2014 2014
dbSNP: rs61902812
rs61902812 		3 1.000 0.080 11 113503698 intergenic variant C/A snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs4936277
rs4936277 		3 1.000 0.080 11 113561238 intergenic variant A/G snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs141424017
rs141424017 		3 1.000 0.080 7 115311376 intergenic variant -/CAA ins 0.700 1.000 1 2019 2019
dbSNP: rs6777876
rs6777876 		3 1.000 0.080 3 11915124 upstream gene variant A/G snv 9.9E-02 0.700 1.000 1 2011 2011
dbSNP: rs1316543
rs1316543
GRK5
3 1.000 0.080 10 119445148 intron variant G/A snv 0.15 0.700 1.000 1 2017 2017
dbSNP: rs2002594
rs2002594
FAM162A
3 1.000 0.080 3 122392714 intron variant A/G snv 0.59 0.700 1.000 1 2017 2017
dbSNP: rs34997829
rs34997829
LHPP
4 1.000 0.080 10 124546821 intron variant G/C snv 0.24 0.700 1.000 1 2017 2017
dbSNP: rs750338
rs750338
PKNOX2
3 1.000 0.080 11 125302697 intron variant A/G snv 0.30 0.700 1.000 1 2011 2011
dbSNP: rs72716801
rs72716801 		3 1.000 0.080 8 127636481 non coding transcript exon variant G/T snv 5.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs1660895
rs1660895 		3 1.000 0.080 2 129236759 intergenic variant A/T snv 0.52 0.700 1.000 1 2014 2014
dbSNP: rs11825659
rs11825659
IGSF9B
4 0.925 0.080 11 133925624 intron variant A/G snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs6716455
rs6716455
LINC01818
3 1.000 0.080 2 150269889 intron variant G/A snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs115460205
rs115460205
FSTL5
3 1.000 0.080 4 161890417 intron variant C/T snv 4.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs17536732
rs17536732
FSTL5
3 1.000 0.080 4 161903214 intron variant G/T snv 4.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs2168784
rs2168784 		3 1.000 0.080 3 164872151 intergenic variant C/T snv 0.24 0.700 1.000 1 2014 2014