Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11740474
GALNT10
1.000 0.040 5 154301187 intron variant A/T snv 0.37 3
rs11765189
PTPRN2
1.000 0.040 7 157743285 intron variant A/G snv 0.25 3
rs12602286
EPN2
1.000 0.040 17 19333641 intron variant G/T snv 0.79 3
rs12704290
GRM3-AS1 ; GRM3
1.000 0.040 7 86798310 intron variant G/A snv 8.9E-02 3
rs13126505
BANK1
1.000 0.040 4 101944147 intron variant G/A snv 4.1E-02 3
rs13262595
LOC107986983 ; TSNARE1
1.000 0.040 8 142235609 intron variant A/C;G snv 3
rs133047
MRTFA
1.000 0.040 22 40631815 intron variant T/C snv 0.93 3
rs1408579
ERLIN1
1.000 0.040 10 100152437 intron variant C/T snv 0.32 3
rs1620977
NEGR1
1.000 0.040 1 72263459 intron variant A/G;T snv 3
rs1711745
INIP
0.925 0.120 9 112690629 intron variant C/A snv 0.13 3
rs2007044
CACNA1C
0.882 0.040 12 2235794 intron variant A/G snv 0.50 3
rs2013208
RBM5 ; RBM6
3 50091966 intron variant C/T snv 0.61 0.56 3
rs2164068
PLCL1
1.000 0.120 2 198079128 intron variant T/A snv 0.52 3
rs2393967
MIR1296 ; JMJD1C
10 63373396 intron variant A/C snv 0.23 3
rs268134
SPRED2
0.925 0.120 2 65381229 intron variant A/C;G;T snv 3
rs28669908
CHRNA3
1.000 0.040 15 78617925 intron variant C/A snv 0.18 3
rs35825582
ARHGAP15
1.000 0.040 2 143491193 intron variant G/A snv 0.45 3
rs4396807
TRIOBP
22 37742372 intron variant G/C snv 0.38 3
rs4664442
SLC4A10
1.000 0.040 2 161971491 intron variant G/A;C snv 3
rs4925114
RAI1
0.925 0.080 17 17807956 intron variant A/G snv 0.53 3
rs4976976
TSNARE1
0.925 0.040 8 142230292 intron variant G/A snv 0.48 3
rs55661361
NRGN
1.000 0.040 11 124744061 intron variant G/A snv 0.43 3
rs59197085
CCDC136
0.925 0.120 7 128820702 intron variant G/A snv 9.9E-02 3
rs62154720
TGFBRAP1
1.000 0.040 2 105306623 intron variant C/T snv 9.2E-02 3
rs62378245
MEF2C-AS1
1.000 0.040 5 89448145 intron variant C/T snv 0.25 3