Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs77960347 18 49583585 missense variant A/C;G snv 4.0E-06; 8.7E-03 5
rs149615216 18 49579658 intron variant C/T snv 5.6E-03 2
rs201922257 18 49569492 missense variant C/T snv 1.7E-04 2.7E-04 2
rs35816125 1.000 0.080 18 49562460 intron variant C/G snv 0.25 2
rs3786247 18 49592553 3 prime UTR variant T/G snv 0.13 2
rs11082764 18 49593209 3 prime UTR variant A/G snv 0.13 1
rs12970066 18 49580782 intron variant C/A;G snv 1