Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7786877 7 100616392 downstream gene variant A/G snv 0.22 2
rs7385804
TFR2
0.851 0.120 7 100638347 intron variant C/A snv 0.65 5
rs4434553
TFR2
1.000 0.040 7 100642568 intron variant A/G snv 0.40 3
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 1
rs9374080
CCDC162P
6 109295217 intron variant T/C snv 0.40 2
rs10207392
ACOXL ; MIR4435-2HG
2 111092082 intron variant A/G snv 0.48 1
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 6
rs2238368
NPRL3
16 120329 intron variant C/T snv 0.36 1
rs7255045
HOOK2
19 12821455 intron variant G/A snv 0.37 2
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 9
rs2853677
TERT
0.724 0.240 5 1287079 3 prime UTR variant G/A snv 0.63 1
rs11085824
GCDH
19 12890733 upstream gene variant A/G snv 0.31 2
rs8176749
ABO
1.000 0.040 9 133255801 synonymous variant C/T snv 0.12 0.11 4
rs8176746
ABO
0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12 3
rs8176743
ABO
1.000 0.040 9 133256028 missense variant C/T snv 0.12 0.11 3
rs8177318
INHCAP ; TF
3 133748533 missense variant T/A snv 1.6E-04 2.9E-04 2
rs12490148
LOC105374116 ; SRPRB
3 133805129 non coding transcript exon variant C/T snv 0.29 1
rs7203560
NPRL3
1.000 0.080 16 134391 intron variant T/G snv 2.0E-02 3
rs9494101
LOC101928277
6 134878458 intergenic variant C/T snv 0.14 3
rs9483769
LOC101928277
6 134878643 intergenic variant A/G;T snv 3
rs6904897
HBS1L
6 135061842 intron variant T/G snv 0.34 1
rs1547247
HBS1L
6 135069698 intron variant G/A snv 0.22 5
rs13220662
HBS1L
6 135074410 intron variant G/A snv 0.41 4