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: rs72973711
rs72973711
ZNF516
1 18 76360290 3 prime UTR variant A/T snv 4.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs28633718
rs28633718
ZNF423
1 16 49850619 intron variant C/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs4703890
rs4703890
ZNF366
1 5 72452797 intron variant G/A snv 0.85 0.700 1.000 1 2019 2019
dbSNP: rs10995249
rs10995249
ZNF365 ; LOC105378327
1 10 62637156 intron variant C/T snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs1474419
rs1474419
ZNF316
1 7 6652974 missense variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs118092853
rs118092853
ZNF235
1 19 44285734 intron variant G/A snv 4.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs58434384
rs58434384
ZNF101
1 19 19675290 intron variant A/G snv 0.12 0.700 1.000 1 2019 2019
dbSNP: rs7832219
rs7832219
ZFPM2 ; ZFPM2-AS1
1 8 105566749 intron variant T/C snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs1350723
rs1350723
ZFPM2
1 8 105218944 intron variant G/A snv 0.69 0.700 1.000 1 2019 2019
dbSNP: rs4782371
rs4782371
ZFPM1
3 1.000 0.040 16 88502423 intron variant T/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs10273974
rs10273974
ZC3HAV1
1 7 139050766 intron variant A/C snv 0.48 0.700 1.000 1 2019 2019
dbSNP: rs73715668
rs73715668
ZC3H3
1 8 143544551 non coding transcript exon variant G/C snv 0.18 0.700 1.000 1 2019 2019
dbSNP: rs4845700
rs4845700
ZBTB7B
1 1 155009232 intron variant C/T snv 0.66 0.700 1.000 1 2011 2011
dbSNP: rs238913
rs238913
ZBTB16
1 11 114113767 intron variant A/G snv 0.46 0.700 1.000 1 2019 2019
dbSNP: rs238914
rs238914
ZBTB16
5 11 114113387 intron variant C/A snv 0.45 0.700 1.000 1 2016 2016
dbSNP: rs2846630
rs2846630
ZBTB16
5 11 114086475 intron variant G/A snv 0.35 0.700 1.000 1 2016 2016
dbSNP: rs878825
rs878825
YDJC
3 22 21627960 upstream gene variant T/C snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs12787996
rs12787996
YAP1
1 11 102186337 non coding transcript exon variant C/A snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs188192
rs188192
XPO6
1 16 28120189 intron variant C/A;T snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs11075747
rs11075747
WWP2
1 16 69906458 intron variant G/A snv 0.47 0.700 1.000 1 2019 2019
dbSNP: rs7025371
rs7025371
WDR31
1 9 113323542 intron variant A/G snv 0.57 0.700 1.000 1 2019 2019
dbSNP: rs28434172
rs28434172
WDR26
1 1 224426923 intron variant C/T snv 0.18 0.700 1.000 1 2019 2019
dbSNP: rs34687215
rs34687215
WDR26
1 1 224394506 intron variant TT/-;T;TTT;TTTTT;TTTTTT;TTTTTTT delins 0.19 0.700 1.000 1 2016 2016
dbSNP: rs17011726
rs17011726
VSTM4
1 10 49056159 intron variant C/G snv 0.18 0.700 1.000 1 2016 2016
dbSNP: rs4272720
rs4272720
VSTM4
2 10 49055156 intron variant A/G snv 0.29 0.700 1.000 1 2019 2019