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: rs10076782
rs10076782
RNF145
1 5 159177955 intron variant G/A snv 0.41 0.800 1.000 1 2011 2011
dbSNP: rs10506328
rs10506328
NFE2
1 12 54293448 intron variant A/C snv 0.75 0.800 1.000 2 2009 2014
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
1 12 54318524 intron variant G/A snv 0.68 0.800 1.000 2 2011 2014
dbSNP: rs10914144
rs10914144
DNM3
3 1 171980610 intron variant T/C snv 0.78 0.800 1.000 4 2009 2014
dbSNP: rs11065987
rs11065987 		12 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs11066301
rs11066301
PTPN11
4 0.827 0.200 12 112433568 intron variant A/G snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs11071720
rs11071720
TPM1 ; TPM1-AS
1 15 63049797 intron variant T/C;G snv 0.800 1.000 2 2009 2016
dbSNP: rs111355755
rs111355755 		1 3 171832858 intron variant G/A snv 0.17 0.700 1.000 1 2012 2012
dbSNP: rs11602954
rs11602954
BET1L
2 11 202856 intron variant G/A snv 0.17 0.800 1.000 2 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
2 1 205275825 intron variant G/A snv 0.30 0.800 1.000 2 2011 2014
dbSNP: rs11734132
rs11734132 		1 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 3 2009 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: rs1354034
rs1354034
ARHGEF3
2 3 56815721 intron variant T/C snv 0.49 0.800 1.000 2 2011 2019
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
dbSNP: rs151361
rs151361
PRELID3B ; SLMO2-ATP5E
1 20 59038947 intron variant A/G snv 0.24 0.700 1.000 1 2012 2012
dbSNP: rs1558324
rs1558324
LOC105369623
1 12 6180053 intergenic variant G/A;C snv 0.800 1.000 1 2011 2011
dbSNP: rs1668873
rs1668873
TMCC2
2 1 205266862 intron variant G/A snv 0.27 0.800 1.000 2 2009 2012
dbSNP: rs16971217
rs16971217
AP2B1
1 17 35617036 intron variant C/A;G snv 0.21 0.800 1.000 1 2011 2011