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: rs964184
rs964184
ZPR1
47 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.700 1.000 2 2016 2019
dbSNP: rs143012756
rs143012756
ZNRF3
2 22 28914537 intron variant G/A snv 3.2E-03 0.700 1.000 1 2019 2019
dbSNP: rs2306589
rs2306589
ZNHIT3
3 17 36493030 non coding transcript exon variant T/C snv 0.49 0.700 1.000 2 2017 2019
dbSNP: rs112134552
rs112134552
ZNF853
2 7 6619030 intron variant G/A snv 9.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs28729203
rs28729203
ZNF800
2 7 127391863 intron variant G/A;C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs12406643
rs12406643
ZNF691
2 1 42845892 intron variant A/G snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs11665661
rs11665661
ZNF611
2 19 52725740 intron variant T/C snv 0.71 0.700 1.000 1 2019 2019
dbSNP: rs4375747
rs4375747
ZNF516
2 18 76359827 3 prime UTR variant C/T snv 5.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs8088980
rs8088980
ZNF407
3 1.000 0.040 18 74666435 intron variant C/T snv 0.51 0.700 1.000 1 2019 2019
dbSNP: rs4811444
rs4811444
ZNF217
2 20 53590524 intron variant T/C snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs571658566
rs571658566
ZNF211
2 19 57632578 intron variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs7080849
rs7080849
ZMIZ1-AS1
2 10 79041217 intron variant T/A;C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs142529006
rs142529006
ZKSCAN1
4 7 100022093 intron variant T/A snv 6.9E-03 0.700 1.000 1 2019 2019
dbSNP: rs28609654
rs28609654
ZFYVE1
2 14 72989530 intron variant T/C snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs11774829
rs11774829
ZFPM2
3 8 104966140 intron variant T/A snv 7.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs74035509
rs74035509
ZFPM1
5 16 88500925 intron variant C/T snv 0.10 0.700 1.000 1 2019 2019
dbSNP: rs927292
rs927292
ZFP36L1
3 1.000 0.120 14 68792124 intron variant C/G snv 0.68 0.700 1.000 1 2019 2019
dbSNP: rs191719058
rs191719058
ZFAND4
2 10 45654497 intron variant T/C snv 1.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs2180414
rs2180414
ZDHHC14
2 6 157461755 intron variant C/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs77786029
rs77786029
ZCCHC8
2 12 122496512 intron variant C/T snv 2.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs11556924
rs11556924
ZC3HC1
21 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 0.700 1.000 1 2019 2019
dbSNP: rs9607793
rs9607793
ZC3H7B
2 22 41340086 missense variant G/A snv 1.3E-02 1.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs12973221
rs12973221
ZC3H4
2 19 47111403 intron variant C/A snv 7.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs2492301
rs2492301
ZC3H12A ; LINC01137
4 1 37473572 intron variant T/C snv 0.53 0.700 1.000 1 2019 2019
dbSNP: rs61827266
rs61827266
ZC3H11A ; ZBED6
2 1 203825625 intron variant G/A snv 0.12 0.700 1.000 1 2019 2019