Disease: Birth Weight
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 7
rs76895963
CCND2-AS1 ; CCND2
1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 6
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 5
rs2292626
PLEKHA1
0.925 0.120 10 122427198 intron variant C/T snv 0.46 3
rs35261542
CDKAL1
1.000 0.080 6 20675561 intron variant C/A snv 0.26 3
rs9379084
RREB1
0.882 0.160 6 7231610 missense variant G/A snv 0.11 8.9E-02 3
rs10814916
GLIS3
0.851 0.200 9 4293150 intron variant A/C snv 0.57 2
rs2421016
PLEKHA1
0.925 0.120 10 122407996 intron variant C/T snv 0.46 2
rs2908279 1.000 0.080 7 44135258 downstream gene variant T/G snv 0.59 2
rs6931514
CDKAL1
0.925 0.120 6 20703721 intron variant A/G snv 0.27 2