Disease: Triglycerides measurement
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 11
rs150844304
TP53BP1
15 43434427 intron variant A/C;G snv 4
rs1936807
RSPO3
6 127127104 intron variant C/G snv 0.55 4