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: rs59499656
rs59499656 		1 18 43188344 intergenic variant A/T snv 0.43 0.700 1.000 2 2018 2018
dbSNP: rs743580
rs743580
PML
1 15 74035775 missense variant A/C;G snv 0.52 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: rs10231365
rs10231365
ITGB8
1 7 20391962 intron variant C/T snv 0.57 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: 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: rs10990303
rs10990303 		1 9 95648123 upstream gene variant C/G;T snv 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: rs11741704
rs11741704 		1 5 8116712 intergenic variant T/A;C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs11913445
rs11913445 		1 22 20154990 upstream gene variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs13192994
rs13192994 		1 6 75529546 intergenic variant A/C snv 0.10 0.700 1.000 1 2017 2017
dbSNP: rs13243553
rs13243553
EXOC4 ; LOC101928861
1 7 133822202 intron variant G/A snv 0.41 0.700 1.000 1 2018 2018
dbSNP: rs13404250
rs13404250
LOC105373786
1 2 187251469 intron variant C/A;G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs13424740
rs13424740
LOC105373786
1 2 187218396 intron variant T/C snv 0.55 0.700 1.000 1 2017 2017
dbSNP: rs1344672
rs1344672
ZBTB38
1 3 141406863 intron variant C/G snv 0.55 0.700 1.000 1 2017 2017
dbSNP: rs1423056
rs1423056 		1 19 33289538 upstream gene variant G/A snv 0.24 0.700 1.000 1 2017 2017
dbSNP: rs1465370
rs1465370 		1 7 130373797 TF binding site variant G/T snv 0.38 0.700 1.000 1 2017 2017
dbSNP: rs149943
rs149943
OR2W2P ; ZSCAN16-AS1
1 6 28034610 non coding transcript exon variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1555091
rs1555091 		1 6 127115500 intron variant G/A snv 0.30 0.700 1.000 1 2017 2017
dbSNP: rs1563352
rs1563352
LYPLAL1-AS1 ; LOC107985272
1 1 219479453 intergenic variant A/C;T snv 0.700 1.000 1 2017 2017