Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10737680
CFH
0.827 0.080 1 196710325 intron variant A/C snv 0.44 7
rs2816992
NR5A2 ; LOC107985244
0.925 0.040 1 200100088 intron variant A/G snv 0.39 4
rs1008833
PIK3C2B
1 204457167 intron variant A/G snv 0.12 3
rs1192415 0.925 0.040 1 91611540 TF binding site variant G/A snv 0.81 3
rs12096239
DHDDS
1 26470431 3 prime UTR variant G/C snv 0.23 3
rs35043843 1 118368672 intergenic variant T/G snv 0.21 3
rs3850625
CACNA1S
1 201047168 missense variant G/A snv 0.12 8.9E-02 3
rs61823192
LYPLAL1-DT
1 219121228 intron variant C/T snv 1.6E-02 3
rs9435733
MFAP2
1 16981759 intron variant T/C snv 0.41 3
rs11264341
TRIM46
0.925 0.120 1 155179017 intron variant C/T snv 0.40 2
rs12737805 1 22286197 regulatory region variant A/G snv 0.20 2
rs1472565
CAPZB
1 19428536 intron variant T/A;C snv 2
rs17009288 1 221030957 regulatory region variant A/C snv 0.30 2
rs187799739
RPRD2
1 150452900 intron variant C/A;G snv 2
rs200154334 1 118319448 regulatory region variant TATA/-;TA;TATATA delins 2
rs28613267 1 218681687 intergenic variant G/C snv 0.49 2
rs3766889
RYR2
1 237778481 intron variant T/G snv 8.4E-02 2
rs4651005
RALGPS2
1 178750171 intron variant C/T snv 0.24 2
rs6681426
ENSA
1 150614495 intron variant G/A snv 0.66 2
rs878471
MCL1 ; ADAMTSL4-AS1
1 150575271 3 prime UTR variant G/A snv 0.48 2
rs9438626
DHDDS
1 26448876 intron variant G/A;C snv 2
rs10157038
CASZ1
1 10652408 non coding transcript exon variant C/A;T snv 1
rs1046874
LOC105371692 ; MDM4
1 204557932 3 prime UTR variant C/T snv 1
rs10779447 1 221587993 intergenic variant A/G snv 0.35 1
rs10914269 1 31096384 upstream gene variant G/T snv 0.70 1