Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16938437
PHF21A
11 46031024 intron variant C/T snv 0.13 2
rs17266097
SATB2
2 199410486 intron variant C/T snv 0.29 2
rs1799949
BRCA1
17 43093449 synonymous variant G/A snv 0.35 0.31 2
rs1861072
UNC80
2 209986910 intron variant T/C snv 0.34 2
rs1933437
FLT3
13 28050157 missense variant G/A snv 0.60 0.53 2
rs2003476
CRTC1
19 18695858 intron variant T/C snv 0.53 2
rs2267958
DNM1
9 128253000 non coding transcript exon variant G/A snv 0.38 2
rs2274465
KDM4A
1 43655886 intron variant C/G snv 0.27 2
rs2679894
TGFBRAP1
2 105254322 upstream gene variant A/G snv 0.43 2
rs3027009
ACKR1 ; CADM3-AS1
1 159204097 intron variant A/G snv 5.8E-02 2
rs3115524
SYCE2 ; GCDH
19 12910545 intron variant G/A;C;T snv 2
rs35436838
RORB
9 74658994 intron variant T/G snv 9.8E-02 2
rs35775580
LOC105375508 ; KLF14
7 130735979 upstream gene variant A/G snv 2.9E-02 2
rs365132
UIMC1
5 176951573 synonymous variant G/T snv 0.51 0.58 2
rs3743266
RORA ; RORA-AS1
15 60489314 3 prime UTR variant T/C snv 0.31 2
rs3784710
MAP2K5
15 67780120 intron variant T/C snv 0.30 2
rs3914188
EEF1AKMT4-ECE2 ; ECE2
3 184292260 3 prime UTR variant G/C snv 0.73 0.73 2
rs4693089
HELQ
4 83452469 intron variant A/G snv 0.60 2
rs4755720
HSD17B12
11 43607199 intron variant C/T snv 0.60 2
rs57149692 16 30130700 regulatory region variant G/C snv 0.46 2
rs6087709 20 35430145 upstream gene variant C/G snv 0.25 2
rs62023121
CHD2
15 92916223 intron variant C/T snv 0.12 2
rs630602
SSBP3
1 54263191 intron variant G/C snv 0.62 2
rs643428
SSBP3
1 54263185 intron variant C/G;T snv 2
rs66461782
ZRANB2-AS1 ; ZRANB2 ; MIR186
1 71067604 intron variant A/T snv 0.32 0.27 2