Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs4795405
LRRC3C
0.851 0.160 17 39932164 intron variant T/A;C snv 6
rs17249437
ARG2 ; GPHN
1.000 0.080 14 67634170 intron variant T/C snv 0.41 2
rs3742879
ARG2 ; GPHN ; VTI1B
1.000 0.080 14 67648284 3 prime UTR variant A/C;G snv 0.21 2
rs967676
CA10
17 51882949 intron variant T/C snv 0.35 1