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: rs10214380
rs10214380 		1 1.000 0.040 5 25946826 intergenic variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs10216809
rs10216809
SGCZ
1 0.925 0.080 8 14507414 intron variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs10228992
rs10228992 		1 1.000 0.040 7 31509640 upstream gene variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs10235204
rs10235204 		1 1.000 0.040 7 104013947 intergenic variant A/C;G snv 0.700 1.000 1 2017 2017
dbSNP: rs10237947
rs10237947
LOC101927914
1 1.000 0.040 7 157465415 upstream gene variant A/C;T snv 0.700 1.000 1 2017 2017
dbSNP: rs10244653
rs10244653
DGKB
1 1.000 0.040 7 14239274 intron variant T/A;G snv 0.700 1.000 1 2017 2017
dbSNP: rs10245061
rs10245061 		1 1.000 0.040 7 85982167 intergenic variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs10248181
rs10248181 		1 1.000 0.040 7 85982497 intergenic variant C/A;G snv 0.700 1.000 1 2017 2017
dbSNP: rs10251943
rs10251943
DPP6
1 1.000 0.040 7 154189530 intron variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs1026666
rs1026666 		1 1.000 0.040 5 99886533 intergenic variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs10279985
rs10279985
GLI3
1 1.000 0.040 7 42232361 intron variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs10306194
rs10306194
PTGS1
1 1.000 0.040 9 122394919 3 prime UTR variant C/A;G snv 0.700 1.000 1 2017 2017
dbSNP: rs1033484
rs1033484
LINC01622
1 1.000 0.040 6 1034909 intron variant A/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs1035760
rs1035760
CNDP2
1 1.000 0.040 18 74517002 non coding transcript exon variant A/G snv 0.700 1.000 1 2017 2017
dbSNP: rs10405183
rs10405183
LOC101927151 ; LOC105372348
1 1.000 0.040 19 27849386 intron variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs10412087
rs10412087
ZNF555
1 1.000 0.040 19 2853568 missense variant A/C;G snv 0.88 0.700 1.000 1 2017 2017
dbSNP: rs10415360
rs10415360
CYP4F12
1 1.000 0.040 19 15680854 non coding transcript exon variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs10421685
rs10421685
HDGFL2
1 1.000 0.040 19 4488929 intron variant G/A;C;T snv 0.700 1.000 1 2017 2017
dbSNP: rs10438809
rs10438809 		1 1.000 0.040 17 27704599 upstream gene variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs10461876
rs10461876 		1 1.000 0.040 5 29907161 intergenic variant G/A;C;T snv 0.700 1.000 1 2017 2017
dbSNP: rs10462547
rs10462547
S100Z
1 1.000 0.040 5 76868587 intron variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs10466537
rs10466537
VWA5A
1 1.000 0.040 11 124135453 intron variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs10469296
rs10469296
PLA2G4C ; PLA2G4C-AS1
1 1.000 0.040 19 48061830 missense variant C/A;T snv 7.2E-06; 0.82 0.700 1.000 1 2017 2017
dbSNP: rs10484021
rs10484021
FOXN3
1 1.000 0.040 14 89409553 intron variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs10486042
rs10486042
DGKB
1 1.000 0.040 7 14229577 intron variant T/C;G snv 0.700 1.000 1 2017 2017