Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10145099
rs10145099
TSHR
1.000 0.120 14 80990350 intron variant C/T snv 0.35
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2011 2011
dbSNP: rs10197319
rs10197319 		1.000 0.120 2 203898321 regulatory region variant G/A;T snv
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2011 2011
dbSNP: rs1044043
rs1044043
TAP2
1.000 0.120 6 32826204 3 prime UTR variant A/C snv 0.82
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2011 2011
dbSNP: rs10908583
rs10908583 		1.000 0.120 1 157671893 downstream gene variant C/T snv 0.57
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2011 2011
dbSNP: rs1149386
rs1149386 		1.000 0.120 1 160471451 TF binding site variant G/C snv 0.96
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2011 2011
dbSNP: rs12050151
rs12050151
CEP128
1.000 0.120 14 80902473 intron variant T/C;G snv
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2011 2011
dbSNP: rs12526548
rs12526548
FGFR1OP
1.000 0.120 6 167017659 intron variant C/T snv 0.43
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2011 2011
dbSNP: rs12743184
rs12743184 		1.000 0.120 1 157784569 intergenic variant A/G snv 0.21
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2011 2011
dbSNP: rs130078
rs130078
CCHCR1
1.000 0.120 6 31150788 synonymous variant C/G snv 0.74 0.75
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2011 2011
dbSNP: rs1610591
rs1610591 		1.000 0.120 6 29710058 upstream gene variant A/G;T snv
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2011 2011
dbSNP: rs17545038
rs17545038
TSHR
1.000 0.120 14 80991228 intron variant T/C snv 0.20
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2011 2011
dbSNP: rs179249
rs179249
TSHR
1.000 0.120 14 80968855 intron variant C/T snv 0.59
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2011 2011
dbSNP: rs1800610
rs1800610
TNF
0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2011 2011
dbSNP: rs204295
rs204295
FGFR1OP
1.000 0.120 6 167087074 intron variant C/T snv 0.50
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2011 2011
dbSNP: rs2050568
rs2050568
FCRL1
0.925 0.160 1 157800451 intron variant C/T snv 0.57
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2011 2011
dbSNP: rs2071652
rs2071652
MOG
1.000 0.120 6 29667540 intron variant C/T snv 4.4E-02
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2011 2011
dbSNP: rs2073723
rs2073723
TCF19
0.925 0.160 6 31162301 intron variant T/C snv 0.78
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2011 2011
dbSNP: rs2075580
rs2075580
DDX39B ; SNORD117 ; ATP6V1G2-DDX39B
1.000 0.120 6 31536198 intron variant G/A;C snv
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2011 2011
dbSNP: rs2210911
rs2210911 		1.000 0.120 1 157674077 downstream gene variant A/G snv 0.46
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2011 2011
dbSNP: rs2217177
rs2217177
CEP128
1.000 0.120 14 80948810 intron variant T/C snv 0.43
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2011 2011
dbSNP: rs2240306
rs2240306 		1.000 0.120 12 48040724 non coding transcript exon variant G/A snv 0.19
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2011 2011
dbSNP: rs2254071
rs2254071 		1.000 0.120 6 29838285 intergenic variant T/C;G snv
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2011 2011
dbSNP: rs2273017
rs2273017
TSBP1 ; TSBP1-AS1
1.000 0.120 6 32369853 intron variant G/A;C snv 0.59
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.800 1.000 1 2011 2011
dbSNP: rs2301436
rs2301436
FGFR1OP
0.752 0.320 6 167024500 intron variant C/T snv 0.42
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2011 2011
dbSNP: rs231804
rs231804 		0.925 0.200 2 203843923 intergenic variant C/T snv 0.60
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2011 2011