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: rs10759102
rs10759102
PTPRD
1 9 9910123 intron variant G/A snv 0.38 0.800 1.000 1 2012 2012
dbSNP: rs12905014
rs12905014 		1 15 92340610 intergenic variant T/C snv 2.4E-02 0.800 1.000 1 2012 2012
dbSNP: rs13144621
rs13144621 		1 4 108296773 intergenic variant T/C snv 0.62 0.800 1.000 1 2012 2012
dbSNP: rs16889038
rs16889038
DCDC2
1 6 24306159 intron variant T/G snv 0.11 0.800 1.000 1 2012 2012
dbSNP: rs17486278
rs17486278
CHRNA5
2 0.827 0.120 15 78575140 intron variant A/C snv 0.32 0.800 1.000 1 2012 2012
dbSNP: rs181654
rs181654 		1 10 117620145 intergenic variant A/G snv 0.62 0.800 1.000 1 2012 2012
dbSNP: rs1997352
rs1997352
RARB
1 3 25496826 intron variant C/A;T snv 0.800 1.000 1 2012 2012
dbSNP: rs2044029
rs2044029
THSD4
1 15 71387620 intron variant A/G snv 0.61 0.800 1.000 1 2012 2012
dbSNP: rs4534959
rs4534959
LINC01924 ; LINC01538
1 18 64209921 intron variant A/G snv 4.2E-02 0.800 1.000 1 2012 2012
dbSNP: rs4767234
rs4767234 		1 12 114200043 intergenic variant A/C;T snv 0.800 1.000 1 2012 2012
dbSNP: rs6684428
rs6684428
LINC01755
1 1 55894140 intron variant T/A snv 0.17 0.800 1.000 1 2012 2012
dbSNP: rs715921
rs715921
SPATA13
1 13 24221351 intron variant G/A snv 0.28 0.800 1.000 1 2012 2012
dbSNP: rs7733088
rs7733088
HTR4 ; LOC107986462
3 1.000 0.040 5 148476770 intron variant G/A;C snv 0.44; 4.1E-06 0.800 1.000 1 2012 2012
dbSNP: rs8031948
rs8031948
HYKK
2 1.000 0.040 15 78523715 intron variant G/T snv 0.27 0.800 1.000 1 2012 2012
dbSNP: rs9536318
rs9536318 		1 13 52920559 intergenic variant G/A snv 0.81 0.800 1.000 1 2012 2012
dbSNP: rs10004908
rs10004908 		1 4 87886094 intergenic variant G/A snv 0.70 0.700 1.000 1 2012 2012
dbSNP: rs10179218
rs10179218 		1 2 117189309 intergenic variant C/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs10778044
rs10778044 		1 12 100184855 intron variant C/T snv 0.94 0.700 1.000 1 2012 2012
dbSNP: rs11111814
rs11111814
TTC41P
1 12 103854918 intron variant T/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs12485367
rs12485367
TMEM212 ; LOC105374218
1 3 171913882 intron variant C/G snv 6.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs12750103
rs12750103 		1 1 21409834 downstream gene variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs132577
rs132577
CACNA1I
1 22 39588081 intron variant A/C;G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs16862394
rs16862394
PFN2
1 3 150037169 intron variant C/T snv 7.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs16992973
rs16992973 		1 20 7028511 intergenic variant G/A snv 6.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs1886467
rs1886467
PRKCH
1 14 61386075 intron variant A/G snv 0.25 0.700 1.000 1 2012 2012