Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16851483
RASA2
0.925 0.080 3 141556594 intron variant G/T snv 6.7E-02 2
rs17020562
RPS6KC1
0.925 0.080 1 213369363 intergenic variant T/C snv 5.9E-02 2
rs17356907
PGAM1P5
0.925 0.080 12 95633983 intron variant A/G snv 0.28 2
rs17467825 0.925 0.080 4 71739800 downstream gene variant A/G snv 0.22 2
rs2284378
RALY
0.851 0.080 20 34000289 intron variant T/C;G snv 2
rs2380205 0.882 0.080 10 5844771 upstream gene variant C/T snv 0.47 2
rs310291 1.000 0.080 8 23801998 downstream gene variant G/A;C snv 2
rs3135724
FGFR2
1.000 0.080 10 121592706 intron variant C/G;T snv 2
rs3853291 1.000 0.080 11 44347927 intergenic variant G/A;C snv 2
rs4342822
LOC105372912 ; PROX1-AS1
0.882 0.080 1 213850882 intron variant G/T snv 0.62 2
rs4849887 0.807 0.080 2 120487546 intergenic variant T/A;C snv 2
rs4930561
KMT5B
0.925 0.080 11 68164294 intron variant G/A snv 0.54 2
rs62061734
MAPT
1.000 0.080 17 45941122 intron variant T/A;C snv 2
rs62235635
PITPNB ; TTC28-AS1 ; MIR3199-2
0.925 0.080 22 27918624 intron variant G/A snv 4.9E-03 2
rs6473252 1.000 0.080 8 80887958 intergenic variant C/T snv 0.33 2
rs6756513 1.000 0.080 2 69945455 downstream gene variant G/A snv 0.26 2
rs6776003
RASA2
1.000 0.080 3 141547651 intron variant G/A snv 0.55 2
rs7072776
MLLT10 ; LOC107984214
0.925 0.080 10 21744013 downstream gene variant A/G snv 0.65 2
rs72932540
LOC338694 ; SMIM38
1.000 0.080 11 69154575 intron variant A/G snv 1.8E-03 2
rs745570 1.000 0.080 17 79807926 intergenic variant A/G snv 0.60 2
rs74949440
TAGLN ; LOC100652768
0.925 0.080 11 117199645 5 prime UTR variant C/G;T snv 1.9E-02 2
rs909116
TNNT3
0.925 0.080 11 1920716 intron variant T/C snv 0.44 2
rs9306160
RRP1B
0.925 0.080 21 43687681 missense variant T/C snv 0.69 0.73 2
rs9397437 1.000 0.080 6 151631197 intergenic variant G/A snv 6.6E-02 2
rs10022462
PPM1K-DT
1.000 0.080 4 88322666 intron variant C/T snv 0.41 1