Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 11
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 10
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 9
rs2571445
TNS1
0.925 0.080 2 217818431 missense variant A/G;T snv 0.62 8
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 7
rs8887
PLIN4 ; HDGFL2
1.000 0.080 19 4502189 3 prime UTR variant T/C;G snv 0.51; 1.8E-05 6
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 6
rs11021221 11 95575690 intron variant T/A;G snv 4
rs113700287
THRB
3 24293020 intron variant -/GTT delins 4
rs159058
NOL4L ; LOC101929698
20 32520305 intron variant A/C;T snv 4
rs56043070
GCSAML
1 247556467 splice donor variant G/A;T snv 5.2E-02; 4.1E-06 4
rs61823972
TMCC2
1 205232197 intron variant A/C;T snv 4
rs754205
IRS2
13 109759295 intron variant A/C;G snv 4
rs778387 1 56158423 intron variant C/A;G;T snv 4
rs8176747
ABO
9 133255928 missense variant C/A;G snv 4.1E-06; 0.12 4
rs113635136
TFRC
3 196075973 intron variant AA/-;A;AAA;AAAA delins 3
rs4832312
RMND5A
2 86762839 intron variant G/A;C snv 3
rs6150565
ANK1
8 41655063 3 prime UTR variant AGAGTCTATACAGC/-;AGAGTCTATACAGCAGAGTCTATACAGC delins 3
rs875741 5 173860848 intergenic variant G/A;C snv 3
rs113525195
PSMB5
14 23030112 intron variant C/A;T snv 2
rs11771301
WIPI2
7 5195031 intron variant C/G;T snv 2
rs1532423
CA1
8 85356084 intron variant A/G;T snv 2
rs2145943 20 39934603 upstream gene variant A/C;G snv 2
rs2307823
H2BC4
6 26118310 intron variant AGATCAGTTTGGTCAA/- delins 2