Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10914144
DNM3
1 171980610 intron variant T/C snv 0.78 3
rs13300663
RCL1
9 4814948 intron variant G/A;C snv 3
rs9376090
HBS1L
6 135090090 intron variant T/C snv 0.19 3
rs10761731
JMJD1C
10 63267850 intron variant A/T snv 0.38 2
rs10974808
RCL1
9 4840380 intron variant A/G snv 9.0E-02 2
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 2
rs11602954
BET1L
11 202856 intron variant G/A snv 0.17 2
rs1354034
ARHGEF3
3 56815721 intron variant T/C snv 0.49 2
rs1668871
TMCC2
1 205268009 intron variant T/C;G snv 2
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 2
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 2
rs4379723
JMJD1C
10 63203689 intron variant T/C snv 0.43 2
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 2
rs7961894
WDR66
12 121927677 intron variant C/T snv 7.3E-02 2
rs8109288
TPM4
19 16074749 non coding transcript exon variant G/A snv 3.9E-02 2
rs8176747
ABO
9 133255928 missense variant C/A;G snv 4.1E-06; 0.12 2
rs944002
EXOC3L4
14 103106478 intron variant A/G snv 0.25 2
rs10058074
MIR3936HG
5 132350453 intron variant G/A snv 0.31 1
rs1034566
ARVCF
22 19996754 intron variant C/G;T snv 1
rs1050316
MEF2D
1 156464911 3 prime UTR variant G/T snv 0.54 1
rs10512472
SLFN14
17 35557785 missense variant T/C snv 0.21 0.19 1
rs10876550
COPZ1
12 54318524 intron variant G/A snv 0.68 1
rs11071720
TPM1-AS ; TPM1
15 63049797 intron variant T/C;G snv 1
rs11628318 14 102573750 regulatory region variant T/A;C snv 1
rs11757577
HBS1L
6 135070327 intron variant G/A;T snv 1