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: rs10862344
rs10862344
PPFIA2
1 1.000 0.040 12 81697021 intron variant A/C snv 0.98 0.700 1.000 1 2017 2017
dbSNP: rs6511404
rs6511404
ZNF730
1 1.000 0.040 19 23105059 intron variant G/A snv 0.98 0.700 1.000 1 2017 2017
dbSNP: rs7507433
rs7507433
ZNF730
1 1.000 0.040 19 23121779 intron variant G/A snv 0.98 0.700 1.000 1 2017 2017
dbSNP: rs2446597
rs2446597
FRMD4A
1 1.000 0.040 10 14007605 intron variant A/G snv 0.98 0.700 1.000 1 2017 2017
dbSNP: rs4486987
rs4486987
ARHGAP28
1 1.000 0.040 18 6762371 intron variant G/A snv 0.98 0.700 1.000 1 2017 2017
dbSNP: rs330033
rs330033 		1 1.000 0.040 8 9243439 intron variant G/A snv 0.98 0.700 1.000 1 2017 2017
dbSNP: rs9840264
rs9840264
FOXP1
1 1.000 0.040 3 71141552 intron variant G/A snv 0.98 0.700 1.000 1 2017 2017
dbSNP: rs243391
rs243391
UBXN6
1 1.000 0.040 19 4449811 non coding transcript exon variant G/A snv 0.98 0.700 1.000 1 2017 2017
dbSNP: rs2053762
rs2053762
LOC105373845
1 1.000 0.040 2 204472387 intron variant A/G snv 0.98 0.700 1.000 1 2017 2017
dbSNP: rs1885645
rs1885645 		1 1.000 0.040 1 177768233 intron variant A/G snv 0.98 0.700 1.000 1 2017 2017
dbSNP: rs12472508
rs12472508 		1 1.000 0.040 2 204456249 intergenic variant G/A snv 0.98 0.700 1.000 1 2017 2017
dbSNP: rs3848860
rs3848860
MYO18B
1 1.000 0.040 22 25790224 intron variant C/T snv 0.98 0.700 1.000 1 2017 2017
dbSNP: rs2842861
rs2842861
SLC25A44
1 1.000 0.040 1 156202708 intron variant T/C snv 0.98 0.700 1.000 1 2017 2017
dbSNP: rs3102718
rs3102718
SCAPER
1 1.000 0.040 15 76752585 intron variant C/T snv 0.98 0.700 1.000 1 2017 2017
dbSNP: rs198260
rs198260 		1 1.000 0.040 14 56714297 intron variant G/A snv 0.98 0.700 1.000 1 2017 2017
dbSNP: rs622180
rs622180 		1 1.000 0.040 19 56080944 downstream gene variant T/C snv 0.98 0.700 1.000 1 2017 2017
dbSNP: rs4273150
rs4273150
C19orf47
1 1.000 0.040 19 40308106 regulatory region variant C/T snv 0.97 0.700 1.000 1 2017 2017
dbSNP: rs2670473
rs2670473
DIAPH3
1 1.000 0.040 13 60078156 intron variant A/G snv 0.97 0.700 1.000 1 2017 2017
dbSNP: rs1550910
rs1550910 		1 1.000 0.040 2 204470907 intron variant C/T snv 0.97 0.700 1.000 1 2017 2017
dbSNP: rs792605
rs792605 		1 1.000 0.040 8 13941525 intergenic variant G/T snv 0.97 0.700 1.000 1 2017 2017
dbSNP: rs9542861
rs9542861 		1 1.000 0.040 13 72147047 intergenic variant T/A snv 0.97 0.700 1.000 1 2017 2017
dbSNP: rs1910462
rs1910462
IQCM
1 1.000 0.040 4 149509171 intron variant G/A snv 0.97 0.700 1.000 1 2017 2017
dbSNP: rs820274
rs820274
GBE1
1 1.000 0.040 3 81496552 intron variant A/G snv 0.97 0.700 1.000 1 2017 2017
dbSNP: rs2959611
rs2959611
ZDHHC2
1 1.000 0.040 8 17218181 intron variant G/A snv 0.97 0.700 1.000 1 2017 2017
dbSNP: rs2718796
rs2718796
TF
1 1.000 0.040 3 133760356 non coding transcript exon variant G/C snv 0.97 0.700 1.000 1 2017 2017