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: rs342293
rs342293
CTB-30L5.1
3 0.882 0.040 7 106731773 intron variant C/G snv 0.42 0.800 1.000 6 2009 2019
dbSNP: rs7961894
rs7961894
WDR66
2 12 121927677 intron variant C/T snv 7.3E-02 0.800 1.000 5 2009 2019
dbSNP: rs1354034
rs1354034
ARHGEF3
4 3 56815721 intron variant T/C snv 0.49 0.800 1.000 4 2011 2019
dbSNP: rs10914144
rs10914144
DNM3
2 1 171980610 intron variant T/C snv 0.78 0.800 1.000 3 2009 2014
dbSNP: rs10506328
rs10506328
NFE2
1 12 54293448 intron variant A/C snv 0.75 0.800 1.000 2 2009 2014
dbSNP: rs11071720
rs11071720
TPM1 ; TPM1-AS
3 15 63049797 intron variant T/C;G snv 0.800 1.000 2 2009 2016
dbSNP: rs11734132
rs11734132 		3 4 6889792 intergenic variant G/C snv 0.17 0.800 1.000 2 2011 2014
dbSNP: rs12485738
rs12485738
ARHGEF3
1 3 56831748 intron variant A/G snv 0.63 0.800 1.000 2 2009 2012
dbSNP: rs2015599
rs2015599
FAR2 ; LOC100506606
2 12 29282547 non coding transcript exon variant G/A snv 0.51 0.800 1.000 2 2011 2016
dbSNP: rs2138852
rs2138852 		1 17 29376331 intron variant C/G;T snv 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: rs8109288
rs8109288
TPM4
2 19 16074749 non coding transcript exon variant G/A snv 3.9E-02 0.800 1.000 2 2011 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: rs10876550
rs10876550
COPZ1
2 12 54318524 intron variant G/A snv 0.68 0.800 1.000 1 2011 2014
dbSNP: rs11602954
rs11602954
BET1L
2 11 202856 intron variant G/A snv 0.17 0.800 1.000 1 2009 2012
dbSNP: rs11653144
rs11653144 		1 17 29348208 upstream gene variant C/T snv 0.43 0.800 1.000 1 2012 2012
dbSNP: rs1172130
rs1172130
TMCC2
1 1 205275825 intron variant G/A snv 0.30 0.800 1.000 1 2011 2014
dbSNP: rs12969657
rs12969657
CD226
1 18 69869260 intron variant C/T snv 0.41 0.800 1.000 1 2011 2011
dbSNP: rs13042885
rs13042885 		2 20 1944061 upstream gene variant C/A;T snv 0.800 1.000 1 2011 2011
dbSNP: rs1473247
rs1473247
RNF145
2 1.000 0.040 5 159176563 intron variant T/C snv 0.41 0.800 1.000 1 2009 2009
dbSNP: rs1558324
rs1558324
LOC105369623
1 12 6180053 intergenic variant G/A;C snv 0.800 1.000 1 2011 2011
dbSNP: rs1668873
rs1668873
TMCC2
1 1 205266862 intron variant G/A snv 0.27 0.800 1.000 1 2009 2012
dbSNP: rs16971217
rs16971217
AP2B1
1 17 35617036 intron variant C/A;G snv 0.21 0.800 1.000 1 2011 2011