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: rs1799990
rs1799990
PRNP
2 0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 0.860 1.000 1 2008 2015
dbSNP: rs1016726
rs1016726
CHN2
1 7 29316787 intron variant G/A snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs10994443
rs10994443
ANK3
2 1.000 0.040 10 60635760 intron variant G/A snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs11136000
rs11136000
CLU
3 0.752 0.160 8 27607002 intron variant T/C snv 0.56 0.700 1.000 1 2012 2012
dbSNP: rs11767557
rs11767557
EPHA1-AS1
2 0.882 0.080 7 143412046 intron variant T/C snv 0.18 0.700 1.000 1 2012 2012
dbSNP: rs12734001
rs12734001
PPP1R12B
2 1.000 0.080 1 202421786 intron variant C/T snv 3.5E-05 0.700 1.000 1 2012 2012
dbSNP: rs12817488
rs12817488
CCDC62
2 1.000 0.040 12 122811747 intron variant G/A snv 0.39 0.700 1.000 1 2012 2012
dbSNP: rs1990622
rs1990622 		1 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 0.700 1.000 1 2012 2012
dbSNP: rs1994090
rs1994090
SLC2A13
2 1.000 0.040 12 40034759 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2075650
rs2075650
TOMM40
20 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.700 1.000 1 2012 2012
dbSNP: rs2736990
rs2736990
SNCA
2 0.882 0.080 4 89757390 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2756271
rs2756271
PRNP ; RPS4XP2
1 20 4684616 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2814707
rs2814707
C9orf72 ; LOC107987057 ; LOC112268043
2 0.882 0.120 9 27536399 non coding transcript exon variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs3764650
rs3764650
ABCA7
2 0.790 0.200 19 1046521 intron variant T/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs3849942
rs3849942
C9orf72 ; LOC107987057
2 0.776 0.200 9 27543283 non coding transcript exon variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs3851179
rs3851179 		3 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 0.700 1.000 1 2012 2012
dbSNP: rs3865444
rs3865444
CD33
2 0.851 0.160 19 51224706 upstream gene variant C/A snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs393152
rs393152
LINC02210 ; LINC02210-CRHR1
5 0.851 0.160 17 45641777 non coding transcript exon variant A/G snv 0.18 0.29 0.700 1.000 1 2012 2012
dbSNP: rs4538475
rs4538475
BST1
2 1.000 0.040 4 15736314 intron variant A/G snv 0.24 0.700 1.000 1 2012 2012
dbSNP: rs597668
rs597668
MARK4 ; BLOC1S3
1 0.925 0.080 19 45205630 intron variant T/A;C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs6052751
rs6052751
RPS4XP2
1 20 4664427 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs6107516
rs6107516
PRNP
2 1.000 0.120 20 4696446 intron variant G/A snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs610932
rs610932
MS4A6A
2 0.851 0.080 11 60171834 downstream gene variant T/G snv 0.57 0.700 1.000 1 2012 2012
dbSNP: rs6116477
rs6116477 		1 20 4704015 downstream gene variant T/C snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs670139
rs670139
MS4A4A ; MS4A4E
1 0.925 0.080 11 60204322 intron variant G/A;T snv 0.700 1.000 1 2012 2012