Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs76076331
PDIA6
1.000 0.040 2 10837459 intron variant C/T snv 1.0E-01 3
rs78381888
ANKRD23 ; CNNM3
0.925 0.040 2 96835038 3 prime UTR variant A/G snv 0.13 3
rs7963801
SYT1
12 79291446 intron variant T/C snv 0.70 3
rs8067165
LOC105376799
17 8128618 upstream gene variant C/A;G;T snv 3
rs9556958
FARP1 ; STK24
1.000 0.040 13 98447792 3 prime UTR variant C/G;T snv 3
rs10129426 14 103552118 upstream gene variant G/A snv 0.54 2
rs10192369 2 160524377 intergenic variant G/A snv 0.45 2
rs10783018
LOC101928219 ; LINC02607
1 95782279 non coding transcript exon variant G/A snv 0.74 2
rs10789285 1.000 0.040 1 69322799 intergenic variant T/G snv 0.33 2
rs10858334
OLFM1
9 135097939 3 prime UTR variant C/A;G snv 9.4E-02 2
rs10922907 1 90727492 downstream gene variant A/G;T snv 2
rs10949662
PTPRN2
7 157741413 intron variant C/A;T snv 2
rs10954772
PURG
8 31006422 intron variant T/A;C snv 2
rs11076962
RBFOX1
16 5761366 intron variant T/C snv 0.25 2
rs1107960 14 54917622 intergenic variant T/A snv 0.42 2
rs11090045
ZC3H7B
1.000 0.040 22 41357599 3 prime UTR variant G/A;C snv 2
rs115024193
LOC105377299 ; BMP2K
4 78793500 intron variant T/A snv 2.3E-02 2
rs11714441
ADCY5
3 123440099 intron variant C/T snv 0.40 2
rs11793831 9 23362313 intron variant G/A;T snv 2
rs12028010 1 41298799 intron variant T/C snv 0.19 2
rs1223397
PHACTR1 ; TBC1D7 ; TBC1D7-LOC100130357
6 13270713 intron variant G/A;C snv 0.19 2
rs12446589
TUFM ; SH2B1
16 28859641 intron variant G/A snv 0.30 2
rs12624433
SLC12A5
1.000 0.040 20 46052214 intron variant G/A snv 0.20 2
rs12653396
LINC00461
1.000 0.040 5 88551455 intron variant T/A snv 0.52 2
rs12761761
PPP2R2D
10 131961871 downstream gene variant C/T snv 0.21 2