Source: GWASCAT ×
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: rs965513
rs965513
PTCSC2
1 0.742 0.200 9 97793827 intron variant A/G;T snv 0.860 1.000 4 2009 2016
dbSNP: rs944289
rs944289 		1 0.742 0.200 14 36180040 upstream gene variant C/T snv 0.45 0.850 1.000 1 2009 2015
dbSNP: rs116909374
rs116909374 		3 0.776 0.120 14 36269155 regulatory region variant C/T snv 2.3E-02 0.840 0.800 2 2012 2017
dbSNP: rs2439302
rs2439302
NRG1
1 0.776 0.200 8 32574851 intron variant G/C snv 0.54 0.830 1.000 1 2012 2015
dbSNP: rs966423
rs966423
DIRC3
1 0.776 0.200 2 217445617 intron variant C/G;T snv 0.820 1.000 1 2012 2013
dbSNP: rs1588635
rs1588635
PTCSC2
1 1.000 0.080 9 97775520 intron variant A/C snv 0.72 0.800 1.000 1 2010 2017
dbSNP: rs6759952
rs6759952
DIRC3
2 1.000 0.080 2 217406996 intron variant T/A;C snv 0.800 1.000 1 2013 2013
dbSNP: rs925489
rs925489
PTCSC2
3 0.882 0.080 9 97784318 intron variant C/T snv 0.71 0.800 1.000 1 2010 2018
dbSNP: rs10069690
rs10069690
TERT
16 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.720 1.000 1 2016 2019
dbSNP: rs7037324
rs7037324
LOC112268051
1 0.882 0.080 9 97896036 regulatory region variant A/G snv 0.71 0.710 1.000 1 2015 2015
dbSNP: rs10122541
rs10122541 		1 1.000 0.080 9 97865986 intergenic variant G/A snv 0.68 0.700 1.000 1 2015 2015
dbSNP: rs11693806
rs11693806
DIRC3
2 0.925 0.120 2 217427435 non coding transcript exon variant C/A;G snv 0.65 0.700 1.000 1 2017 2017
dbSNP: rs12129938
rs12129938
PCNX2
1 1.000 0.080 1 233276815 intron variant A/G snv 0.20 0.700 1.000 1 2017 2017
dbSNP: rs2289261
rs2289261
SMAD3
1 1.000 0.080 15 67165147 intron variant G/C;T snv 0.61 0.700 1.000 1 2017 2017
dbSNP: rs2466076
rs2466076
NRG1
1 1.000 0.080 8 32575278 intron variant G/T snv 0.53 0.700 1.000 1 2017 2017
dbSNP: rs368187
rs368187
LOC105370452
1 0.925 0.080 14 36063370 non coding transcript exon variant G/A;C;T snv 0.700 1.000 1 2017 2017
dbSNP: rs56062135
rs56062135
SMAD3
6 0.790 0.200 15 67163292 intron variant C/T snv 0.18 0.700 1.000 1 2017 2017
dbSNP: rs6793295
rs6793295
LRRC34
5 0.827 0.240 3 169800667 missense variant T/C;G snv 0.37; 1.8E-04 0.700 1.000 1 2017 2017
dbSNP: rs73227498
rs73227498
EPB41L4A
1 1.000 0.080 5 112150207 intron variant A/T snv 0.11 0.700 1.000 1 2017 2017
dbSNP: rs7902587
rs7902587 		2 0.925 0.080 10 103934543 intergenic variant C/T snv 0.11 0.700 1.000 1 2017 2017