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: rs55657917
rs55657917
LINC02210-CRHR1
1 17 45767194 intron variant T/G snv 0.14 0.700 1.000 2 2018 2018
dbSNP: rs10080237
rs10080237
BCKDHB
1 6 80144753 intron variant T/C snv 0.36 0.700 1.000 1 2017 2017
dbSNP: rs10101061
rs10101061
LOC107986930
1 8 23735787 intron variant T/A snv 0.30 0.700 1.000 1 2017 2017
dbSNP: rs10195252
rs10195252
COBLL1
7 0.925 0.080 2 164656581 intron variant T/C snv 0.48 0.700 1.000 1 2017 2017
dbSNP: rs10231365
rs10231365
ITGB8
1 7 20391962 intron variant C/T snv 0.57 0.700 1.000 1 2017 2017
dbSNP: rs10482795
rs10482795
TGFB2
2 1 218432267 intron variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs10510554
rs10510554
RARB
2 3 25058285 intron variant T/C snv 0.53 0.700 1.000 1 2017 2017
dbSNP: rs10786152
rs10786152
PLCE1
1 10 94133757 intron variant A/G snv 0.49 0.700 1.000 1 2017 2017
dbSNP: rs10842707
rs10842707 		4 12 26318431 intron variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs10842708
rs10842708 		2 12 26321934 intron variant G/A snv 0.62 0.700 1.000 1 2017 2017
dbSNP: rs10843151
rs10843151
CCDC91
1 12 28318386 intron variant G/A snv 0.20 0.700 1.000 1 2017 2017
dbSNP: rs10849145
rs10849145
KCNA6 ; GALNT8 ; LOC105369614
1 12 4808002 intron variant T/C snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs10876528
rs10876528
HOXC4 ; HOXC5 ; HOXC6
2 12 54027692 intron variant C/A;G snv 0.700 1.000 1 2017 2017
dbSNP: rs10923712
rs10923712
TBX15
4 1 118962811 intron variant G/A snv 0.56 0.700 1.000 1 2017 2017
dbSNP: rs10968577
rs10968577
LINGO2
3 9 28415514 intron variant C/T snv 0.27 0.700 1.000 1 2017 2017
dbSNP: rs11057397
rs11057397
CCDC92 ; DNAH10
1 12 123935181 intron variant C/T snv 0.32 0.700 1.000 1 2017 2017
dbSNP: rs11156429
rs11156429
LIN28B-AS1
1 6 104916546 intron variant T/G snv 0.46 0.700 1.000 1 2017 2017
dbSNP: rs111901094
rs111901094
GATAD2A
1 19 19402761 intron variant G/T snv 4.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs11209951
rs11209951
LOC105378797
3 1 72371807 intron variant C/T snv 0.61 0.700 1.000 1 2017 2017
dbSNP: rs11672660
rs11672660
GIPR ; MIR642B
5 19 45676926 intron variant C/T snv 0.18 0.17 0.700 1.000 1 2017 2017
dbSNP: rs11694842
rs11694842
DNMT3A
2 2 25260101 intron variant A/G snv 0.22 0.700 1.000 1 2017 2017
dbSNP: rs117911989
rs117911989
MKLN1
2 7 131285034 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs11897119
rs11897119
MEIS1
3 2 66544868 intron variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs12317176
rs12317176
CCDC92 ; DNAH10
3 12 123920171 intron variant T/C snv 0.39 0.700 1.000 1 2017 2017
dbSNP: rs12330322
rs12330322
RYBP
2 3 72406204 intron variant C/A;T snv 0.700 1.000 1 2017 2017