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
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 10
rs2189234
TET2
1.000 0.040 4 105154341 intron variant T/G snv 0.62 3
rs670523
RIT1
1.000 0.040 1 155908941 intron variant A/G snv 0.48 3