Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11008222 0.925 0.080 10 30753565 intergenic variant G/A snv 0.39 2
rs77471149 0.925 0.080 4 167914184 intergenic variant A/C;G snv 2
rs8061121
C16orf95
0.925 0.080 16 87159478 intron variant T/C snv 0.89 2
rs12045807
ENSA
0.925 0.080 1 150612358 intron variant T/C snv 0.18 2
rs104893965
GJA1
0.925 0.080 6 121447974 missense variant G/A snv 2.0E-04 1.8E-04 2
rs2227885
GJA1
0.925 0.080 6 121447932 missense variant G/A snv 4.2E-04 1.3E-04 2
rs1642645
HIVEP3
0.925 0.080 1 42036610 intron variant A/C snv 0.80 2
rs72820264
HULC
0.925 0.080 6 9291650 intron variant T/C snv 0.15 2
rs11894932
MGAT4A
0.925 0.080 2 98648723 intron variant A/C snv 0.21 2
rs3746446
MYH7B
0.925 0.080 20 34986962 synonymous variant T/C snv 0.19 0.18 2
rs55788414
PKD1L2
0.925 0.080 16 81151334 intron variant C/T snv 6.3E-02 2
rs1975649
SYNPR ; SYNPR-AS1
0.925 0.080 3 63453210 intron variant T/C snv 0.74 2