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: rs1343795
rs1343795
ZNF652
5 0.882 0.120 17 49334880 intron variant C/A snv 0.78 0.010 1.000 1 2018 2018
dbSNP: rs4572450
rs4572450
ZNF652
4 0.882 0.120 17 49343367 intron variant T/C snv 0.78 0.010 1.000 1 2018 2018
dbSNP: rs10995251
rs10995251
ZNF365 ; LOC105378327
1 1.000 0.120 10 62638706 intron variant C/T snv 0.29 0.800 1.000 1 2012 2012
dbSNP: rs2393903
rs2393903
ZNF365
1 1.000 0.120 10 62620576 intron variant T/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs2944542
rs2944542
ZNF365
2 0.925 0.120 10 62610240 intron variant C/G snv 0.71 0.700 1.000 1 2015 2015
dbSNP: rs73510898
rs73510898
ZGLP1
2 0.925 0.120 19 10305768 intron variant G/A;C;T snv 0.700 1.000 1 2015 2015
dbSNP: rs512685
rs512685
ZC3H12D
1 1.000 0.120 6 149471889 intron variant G/A snv 0.15 0.700 1.000 1 2011 2011
dbSNP: rs6720763
rs6720763
XIRP2 ; XIRP2-AS1
1 1.000 0.120 2 167135776 intron variant T/C snv 0.27 0.700 1.000 1 2015 2015
dbSNP: rs612529
rs612529
VSTM1
2 0.925 0.120 19 54063999 upstream gene variant A/G;T snv 0.010 1.000 1 2017 2017
dbSNP: rs1544410
rs1544410
VDR
78 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.020 1.000 2 2016 2020
dbSNP: rs731236
rs731236
VDR
81 0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 0.020 1.000 2 2013 2020
dbSNP: rs2228570
rs2228570
VDR
99 0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 0.010 < 0.001 1 2013 2013
dbSNP: rs1893592
rs1893592
UBASH3A
12 0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs1898671
rs1898671
TSLP
5 0.851 0.160 5 111072304 intron variant C/T snv 0.25 0.010 1.000 1 2019 2019
dbSNP: rs2289278
rs2289278
TSLP
5 0.827 0.200 5 111073450 5 prime UTR variant C/G snv 8.7E-02 0.010 1.000 1 2016 2016
dbSNP: rs9469099
rs9469099
TSBP1 ; TSBP1-AS1
1 1.000 0.120 6 32341131 intron variant G/A;T snv 0.800 1.000 1 2012 2012
dbSNP: rs12153855
rs12153855
TNXB
11 0.776 0.320 6 32107027 intron variant T/C snv 0.11 0.800 1.000 1 2013 2013
dbSNP: rs12198173
rs12198173
TNXB
9 0.827 0.240 6 32059031 intron variant G/A snv 0.10 0.700 1.000 1 2013 2013
dbSNP: rs12211410
rs12211410
TNXB
5 0.925 0.120 6 32081646 missense variant C/G;T snv 5.6E-05; 7.7E-02; 3.7E-05 0.700 1.000 1 2013 2013
dbSNP: rs13199524
rs13199524
TNXB
9 0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 0.700 1.000 1 2013 2013
dbSNP: rs41268896
rs41268896
TNXB
1 1.000 0.120 6 32102292 intron variant G/A snv 0.25 0.700 1.000 1 2015 2015
dbSNP: rs909341
rs909341
TNFRSF6B ; RTEL1-TNFRSF6B
1 1.000 0.120 20 63697389 synonymous variant C/T snv 0.25 0.19 0.700 1.000 1 2015 2015
dbSNP: rs102275
rs102275
TMEM258
18 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 0.010 1.000 1 2015 2015
dbSNP: rs13360927
rs13360927
TMEM232
3 0.882 0.160 5 110700055 intron variant A/G snv 9.3E-02 0.710 1.000 2 2011 2012
dbSNP: rs13361382
rs13361382
TMEM232
3 0.882 0.160 5 110713253 intron variant G/A snv 9.3E-02 0.710 1.000 2 2011 2012