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: rs445
rs445
CDK6
9 7 92779056 intron variant C/T snv 0.14 0.800 1.000 4 2011 2019
dbSNP: rs12619285
rs12619285
LOC102725082
3 1.000 0.040 2 212959321 intron variant A/G snv 0.31 0.800 1.000 3 2009 2019
dbSNP: rs1036332
rs1036332
LINC01221
3 1 199043349 intron variant A/C snv 0.70 0.700 1.000 2 2016 2019
dbSNP: rs11204682
rs11204682
ENSA
4 1 150623061 intron variant G/A;T snv 0.700 1.000 2 2016 2019
dbSNP: rs113473633
rs113473633
NFKB1
4 1.000 0.040 4 102527974 intron variant A/G snv 1.6E-02 0.700 1.000 2 2016 2019
dbSNP: rs114269697
rs114269697
JAK1
3 1.000 0.040 1 64848529 intron variant C/A snv 7.3E-03 0.700 1.000 2 2016 2019
dbSNP: rs12705849
rs12705849
LOC107986837
1 7 113142501 intron variant G/A snv 0.32 0.700 1.000 2 2016 2019
dbSNP: rs150640087
rs150640087
IKZF1
2 7 50376454 intron variant G/T snv 1.0E-02 0.700 1.000 2 2016 2019
dbSNP: rs159963
rs159963
RERE
3 1.000 0.040 1 8444361 intron variant C/A snv 0.52 0.700 1.000 2 2016 2019
dbSNP: rs16917546
rs16917546
ZNF365 ; LOC105378327
6 0.851 0.040 10 62637778 intron variant T/C snv 0.29 0.700 1.000 2 2018 2019
dbSNP: rs1695315
rs1695315
IL5RA
1 3 3111655 intron variant G/A snv 0.56 0.700 1.000 2 2016 2019
dbSNP: rs17758695
rs17758695
BCL2
10 18 63253621 intron variant C/T snv 2.1E-02 0.700 1.000 2 2016 2019
dbSNP: rs2296618
rs2296618
PTPRC
2 1 198697103 intron variant A/G snv 0.21 0.700 1.000 2 2016 2019
dbSNP: rs2960422
rs2960422
PPARG
2 1.000 0.080 3 12293492 intron variant G/A snv 0.59 0.700 1.000 2 2016 2019
dbSNP: rs34290285
rs34290285
D2HGDH
8 0.851 0.120 2 241759225 intron variant G/A snv 0.27 0.700 1.000 2 2016 2019
dbSNP: rs410867
rs410867 		2 19 16316300 intron variant A/G snv 0.32 0.700 1.000 2 2016 2019
dbSNP: rs61612642
rs61612642
TRERF1
2 6 42229969 intron variant C/T snv 0.21 0.700 1.000 2 2016 2019
dbSNP: rs62408225
rs62408225
BACH2
2 1.000 0.120 6 90246690 intron variant A/G snv 0.26 0.700 1.000 2 2016 2019
dbSNP: rs7288670
rs7288670
GGT5
4 22 24225858 intron variant A/C;G snv 0.700 1.000 2 2016 2019
dbSNP: rs73072483
rs73072483
DOCK3
2 3 50734193 intron variant G/A snv 9.6E-02 0.700 1.000 2 2016 2019
dbSNP: rs7569084
rs7569084
SPRED2
2 2 65429835 intron variant C/T snv 0.62 0.700 1.000 2 2016 2019
dbSNP: rs9504361
rs9504361
EXOC2
3 1.000 0.040 6 577820 intron variant A/G snv 0.40 0.700 1.000 2 2016 2019
dbSNP: rs960709
rs960709
TNIP1
5 0.882 0.120 5 151081488 intron variant A/G;T snv 0.700 1.000 2 2016 2019
dbSNP: rs9829778
rs9829778
PAK2
2 3 196822218 intron variant G/A snv 0.53 0.700 1.000 2 2016 2019
dbSNP: rs9900933
rs9900933
UNK
3 17 75805073 intron variant T/A;C;G snv 0.700 1.000 2 2016 2019