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: rs17023459
rs17023459
AFF3
1 2 100067088 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs9557386
rs9557386
PCCA
1 13 100115087 intron variant C/G snv 0.33 0.700 1.000 1 2018 2018
dbSNP: rs6709656
rs6709656
AFF3
1 2 100190257 intron variant A/G snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs2309757
rs2309757
AFF3
1 2 100191263 intron variant T/C snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs71413877
rs71413877
LONRF2
2 2 100308360 intron variant G/A snv 2.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs10183150
rs10183150
LONRF2
1 2 100322655 upstream gene variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10164820
rs10164820 		1 2 100433891 intergenic variant G/C snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs34106693
rs34106693 		1 2 100535368 intergenic variant C/G snv 0.11 0.700 1.000 1 2018 2018
dbSNP: rs9513780
rs9513780
TMTC4
1 13 100666927 intron variant C/T snv 0.37 0.700 1.000 1 2018 2018
dbSNP: rs2942884
rs2942884 		1 2 100707116 regulatory region variant G/A snv 0.50 0.700 1.000 1 2018 2018
dbSNP: rs1693584
rs1693584
LOC105375673
1 8 100736689 downstream gene variant T/C snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs4906037
rs4906037
LOC105370670
1 14 101076143 splice region variant T/C snv 0.71 0.700 1.000 1 2018 2018
dbSNP: rs6421896
rs6421896 		1 5 101205761 intergenic variant A/G snv 0.71 0.700 1.000 1 2018 2018
dbSNP: rs72776049
rs72776049
GRIN2A
1 16 10127597 intron variant T/C snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs58764043
rs58764043
MSRA
1 8 10148373 intron variant C/T snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs6575858
rs6575858 		1 14 101565415 upstream gene variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs2895917
rs2895917 		1 14 101586438 intergenic variant C/T snv 0.32 0.700 1.000 1 2018 2018
dbSNP: rs12380816
rs12380816
GRIN3A
1 9 101651388 intron variant T/C snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs1337415
rs1337415
GRIK2
1 6 101664650 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs749694
rs749694
LOC105378458
2 10 101760027 regulatory region variant A/G snv 0.45 0.700 1.000 1 2018 2018
dbSNP: rs2529207
rs2529207 		1 7 101780519 intergenic variant C/T snv 0.32 0.700 1.000 1 2018 2018
dbSNP: rs2735421
rs2735421
FGF8 ; NPM3
2 10 101781259 upstream gene variant T/G snv 0.65 0.700 1.000 1 2018 2018
dbSNP: rs8046217
rs8046217 		1 16 10195005 intergenic variant T/A snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs401966
rs401966
CUX1
1 7 102052537 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs61874768
rs61874768
LDB1 ; PPRC1
2 10 102120361 5 prime UTR variant G/A;T snv 0.700 1.000 1 2018 2018