Source: GWASDB ×
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: rs342293
rs342293
CTB-30L5.1
1 0.882 0.040 7 106731773 intron variant C/G snv 0.42 0.800 1.000 5 2009 2019
dbSNP: rs12485738
rs12485738
ARHGEF3
1 3 56831748 intron variant A/G snv 0.63 0.800 1.000 3 2009 2012
dbSNP: rs2138852
rs2138852 		1 17 29376331 intron variant C/G;T snv 0.800 1.000 3 2009 2012
dbSNP: rs10506328
rs10506328
NFE2
1 12 54293448 intron variant A/C snv 0.75 0.800 1.000 2 2009 2014
dbSNP: rs10876550
rs10876550
COPZ1
1 12 54318524 intron variant G/A snv 0.68 0.800 1.000 2 2011 2014
dbSNP: rs11071720
rs11071720
TPM1 ; TPM1-AS
1 15 63049797 intron variant T/C;G snv 0.800 1.000 2 2009 2016
dbSNP: rs11734132
rs11734132 		1 4 6889792 intergenic variant G/C snv 0.17 0.800 1.000 2 2011 2014
dbSNP: rs201800621
rs201800621
CD226
1 18 69849609 intron variant G/A;C snv 0.700 1.000 2 2009 2012
dbSNP: rs2393967
rs2393967
JMJD1C ; MIR1296
1 10 63373396 intron variant A/C snv 0.23 0.800 1.000 2 2009 2012
dbSNP: rs6136489
rs6136489 		1 20 1943088 upstream gene variant T/G snv 0.46 0.800 1.000 2 2009 2012
dbSNP: rs647316
rs647316
EHD3
1 2 31241963 intron variant A/G snv 0.80 0.800 1.000 2 2009 2012
dbSNP: rs7075195
rs7075195
JMJD1C
1 10 63290899 intron variant A/G snv 0.38 0.800 1.000 2 2011 2014
dbSNP: rs75761474
rs75761474
CD226
1 18 69849610 intron variant A/- del 0.53 0.700 1.000 2 2009 2012
dbSNP: rs8076739
rs8076739 		1 17 29387569 intron variant C/T snv 0.64 0.800 1.000 2 2011 2014
dbSNP: rs893001
rs893001
CD226
1 18 69849610 intron variant A/C snv 0.18 0.800 1.000 2 2009 2012
dbSNP: rs10076782
rs10076782
RNF145
1 5 159177955 intron variant G/A snv 0.41 0.800 1.000 1 2011 2011
dbSNP: rs10512627
rs10512627
KALRN
1 3 124621375 intron variant G/C snv 0.43 0.800 1.000 1 2011 2011
dbSNP: rs10813766
rs10813766
DOCK8
1 9 331490 intron variant T/G snv 0.64 0.800 1.000 1 2011 2011
dbSNP: rs111355755
rs111355755 		1 3 171832858 intron variant G/A snv 0.17 0.700 1.000 1 2012 2012
dbSNP: rs11653144
rs11653144 		1 17 29348208 upstream gene variant C/T snv 0.43 0.800 1.000 1 2012 2012
dbSNP: rs12526480
rs12526480
CARMIL1
1 6 25533306 intron variant T/G snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs12969657
rs12969657
CD226
1 18 69869260 intron variant C/T snv 0.41 0.800 1.000 1 2011 2011
dbSNP: rs13042885
rs13042885 		1 20 1944061 upstream gene variant C/A;T snv 0.800 1.000 1 2011 2011
dbSNP: rs13236689
rs13236689
CD36
1 7 80606698 intron variant T/G snv 0.44 0.700 1.000 1 2012 2012
dbSNP: rs1473247
rs1473247
RNF145
1 1.000 0.040 5 159176563 intron variant T/C snv 0.41 0.800 1.000 1 2009 2009