Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs572169
GHSR
0.882 0.160 3 172447937 synonymous variant C/T snv 0.31 0.24 6
rs5574
NPY ; LOC107986777
0.882 0.200 7 24289514 synonymous variant C/T snv 0.43 0.43 5
rs1051168
NMB
1.000 0.080 15 84657289 missense variant G/C;T snv 4.5E-06; 0.22 2
rs992472
DNMT3B
20 32797463 intron variant G/T snv 0.49 1
rs992990
GAD2
10 26278252 intron variant C/A;G snv 0.37 1
rs781443388
NPY2R
4 155214416 synonymous variant G/A snv 1.6E-05 2.1E-05 1
rs2878329
OR7D4
19 9215066 intron variant C/T snv 0.14 1
rs1258628899
PYY
17 43953174 synonymous variant G/A snv 7.0E-06 1