Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs2229616
MC4R
0.732 0.200 18 60372043 missense variant C/T snv 1.6E-02 1.6E-02 22
rs104894845
GLA ; RPL36A-HNRNPH2
0.807 0.160 X 101401752 missense variant C/G;T snv 5.5E-04 8
rs9937053
FTO
0.882 0.160 16 53765595 intron variant G/A snv 0.42 6
rs1555728965
NOTCH3
0.925 0.080 19 15188277 missense variant A/C snv 4
rs797045014
NOTCH3
0.851 0.160 19 15192182 missense variant G/A;T snv 4