Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 9
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 7
rs2235544
DIO1
0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 2
rs11012732
MLLT10
0.882 0.080 10 21541175 intron variant A/G snv 0.31 1
rs1243180
MLLT10
0.790 0.160 10 21626690 intron variant T/A snv 0.23 1
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 1