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: rs6684992
rs6684992 		2 1 87286317 intergenic variant A/T snv 0.20 0.700 1.000 2 2016 2018
dbSNP: rs6920211
rs6920211
LOC105378010
4 6 135110180 regulatory region variant T/C snv 0.29 0.700 1.000 2 2016 2019
dbSNP: rs7080536
rs7080536
HABP2 ; NRAP
27 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 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: rs74480102
rs74480102
KDM6B
3 17 7839283 upstream gene variant G/A snv 2.5E-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: rs8179
rs8179
CDK6
8 0.882 0.080 7 92606850 3 prime UTR variant T/A;C;G snv 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
dbSNP: rs9979383
rs9979383
RUNX1
5 0.925 0.200 21 35343463 intron variant C/G;T snv 0.700 1.000 2 2016 2019
dbSNP: rs1000005
rs1000005
LINC00945
1 21 33060745 intron variant G/C snv 0.51 0.700 1.000 1 2016 2016
dbSNP: rs10045577
rs10045577
WDR36
1 5 111090753 intron variant C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1004870
rs1004870
HIVEP3
1 1 41905116 intron variant C/T snv 0.57 0.700 1.000 1 2019 2019
dbSNP: rs10075801
rs10075801
SLC22A4 ; MIR3936HG
5 5 132341949 intron variant A/G snv 0.31 0.700 1.000 1 2016 2016
dbSNP: rs10083558
rs10083558
CRTC3-AS1 ; LINC01585
1 15 90659273 intron variant C/A snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs10118552
rs10118552 		1 9 90004338 intron variant A/G snv 0.59 0.700 1.000 1 2019 2019
dbSNP: rs10135205
rs10135205
LOC105370686 ; LOC105378183
1 14 103316504 regulatory region variant A/G snv 0.54 0.700 1.000 1 2019 2019
dbSNP: rs10138752
rs10138752
RAD51B
5 14 68713254 intron variant C/T snv 8.8E-02 0.700 1.000 1 2016 2016
dbSNP: rs1013910
rs1013910 		1 1 116868761 intergenic variant G/A snv 0.91 0.700 1.000 1 2019 2019
dbSNP: rs10147992
rs10147992
STXBP6
3 14 25034593 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs10165200
rs10165200
LINC00299
2 2 8299499 intron variant G/A snv 0.36 0.700 1.000 1 2016 2016
dbSNP: rs10173538
rs10173538
BAZ2B ; MARCHF7
5 2 159712765 intron variant C/G;T snv 0.700 1.000 1 2016 2016