Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2066938
UNC119B ; MIR4700
12 120722812 3 prime UTR variant A/C;G snv 3
rs55730005
UNC119B
12 120719733 intron variant C/A;G snv 2
rs17847
UNC119B
12 120711672 non coding transcript exon variant A/G snv 0.60 1
rs34734847
UNC119B
12 120716418 intron variant T/C snv 0.38 1
rs3833788
UNC119B
12 120713260 splice acceptor variant CTCTTGT/-;CTCTTGTCTCTTGT delins 0.37 1
rs556001
UNC119B
12 120715164 intron variant A/G snv 0.45 1
rs56273049
UNC119B
12 120718238 intron variant A/T snv 0.38 1
rs696337
UNC119B ; MIR4700
12 120721577 3 prime UTR variant T/C snv 0.60 1