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: rs60086424
rs60086424
LOC730100
1 1.000 0.120 2 52162981 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs6021191
rs6021191
NFATC2
5 0.851 0.120 20 51419700 intron variant A/T snv 4.9E-02 0.700 1.000 1 2015 2015
dbSNP: rs60218192
rs60218192
HS3ST4
1 1.000 0.120 16 25874649 intron variant G/A;C snv 8.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs6479778
rs6479778
ARID5B
5 0.827 0.200 10 61929318 intron variant T/C;G snv 0.010 1.000 1 2017 2017
dbSNP: rs6550253
rs6550253
LINC01811
3 1.000 0.120 3 34149739 intron variant G/A snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs6951648
rs6951648
DDC ; FIGNL1
1 1.000 0.120 7 50499795 intron variant G/A snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs7073837
rs7073837
ARID5B
4 0.851 0.120 10 61940136 intron variant A/C snv 0.58 0.64 0.700 1.000 1 2013 2013
dbSNP: rs7075634
rs7075634
PIP4K2A
1 1.000 0.120 10 22564173 intron variant T/C snv 0.57 0.700 1.000 1 2013 2013
dbSNP: rs7087125
rs7087125
ARID5B
1 1.000 0.120 10 62013280 intron variant C/T snv 0.37 0.700 1.000 1 2013 2013
dbSNP: rs7088318
rs7088318
PIP4K2A
4 0.851 0.120 10 22564019 intron variant C/A snv 0.55 0.700 1.000 1 2013 2013
dbSNP: rs7142143
rs7142143
PYGL
1 1.000 0.120 14 50936813 intron variant T/C snv 2.8E-02 0.800 1.000 1 2012 2012
dbSNP: rs7156960
rs7156960
GPATCH2L ; LOC105370575
1 1.000 0.120 14 76237008 intron variant C/G;T snv 0.800 1.000 1 2012 2012
dbSNP: rs72772090
rs72772090
CAST
3 1.000 0.120 5 96700607 intron variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs73062673
rs73062673
CNOT3 ; LOC102724273
1 1.000 0.120 19 54151243 intron variant T/C snv 1.0E-01 0.700 1.000 1 2019 2019
dbSNP: rs74709575
rs74709575
LINC02334
3 1.000 0.120 13 38041119 intron variant A/C snv 3.1E-03 0.700 1.000 1 2017 2017
dbSNP: rs755622
rs755622
MIF ; MIF-AS1
44 0.611 0.720 22 23894205 intron variant G/C snv 0.26 0.010 1.000 1 2018 2018
dbSNP: rs7791875
rs7791875
DDC ; FIGNL1
1 1.000 0.120 7 50503190 intron variant C/T snv 1.0E-01 0.700 1.000 1 2013 2013
dbSNP: rs7803247
rs7803247
DDC ; FIGNL1
1 1.000 0.120 7 50473045 intron variant T/C snv 0.52 0.700 1.000 1 2013 2013
dbSNP: rs7806674
rs7806674
IKZF1
1 1.000 0.120 7 50356265 intron variant C/A;G snv 0.700 1.000 1 2013 2013
dbSNP: rs7808025
rs7808025
DDC ; FIGNL1
1 1.000 0.120 7 50509205 intron variant G/A;C snv 0.28 0.700 1.000 1 2013 2013
dbSNP: rs7818688
rs7818688
NDUFAF6
3 1.000 0.120 8 95011854 intron variant C/A;G snv 0.700 1.000 1 2015 2015
dbSNP: rs7901152
rs7901152
PIP4K2A
1 1.000 0.120 10 22544224 intron variant G/A snv 0.66 0.700 1.000 1 2013 2013
dbSNP: rs79050301
rs79050301
TPMT
1 1.000 0.120 6 18151959 intron variant T/C snv 4.5E-02 0.700 1.000 1 2018 2018
dbSNP: rs7923074
rs7923074
ARID5B
1 1.000 0.120 10 61963681 intron variant A/C snv 0.56 0.700 1.000 1 2013 2013
dbSNP: rs924607
rs924607
LOC100996325 ; LOC105374608
7 0.851 0.120 5 609978 intron variant C/T snv 0.32 0.700 1.000 1 2015 2015