Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs201111080
PAPPA2
1 176670971 missense variant G/T snv 1.9E-04 1.8E-04 1
rs7330796
TBC1D4
13 75324027 intron variant T/C snv 0.76 1
rs17271305
VPS13C
15 62040781 intron variant A/G;T snv 1