Disease: Body Height
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7195386
RBBP6
0.925 0.120 16 24567137 splice region variant T/A;C snv 0.56 2
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs7740107
L3MBTL3
1.000 0.080 6 130053316 intron variant T/A;G snv 6
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 20
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 4
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 8
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs7826312
NRG1
8 32542597 intron variant T/C snv 0.57 2
rs76895963
CCND2-AS1 ; CCND2
1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 6