Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2274223
PLCE1
0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 40
rs3765524
PLCE1
0.724 0.320 10 94298541 missense variant C/T snv 0.27 0.31 17
rs7922612
PLCE1
0.752 0.080 10 94051682 intron variant C/T snv 0.39 14
rs2274224
PLCE1-AS1 ; PLCE1
0.882 0.080 10 94279840 missense variant G/A;C snv 8.8E-05; 0.44 6
rs11599672
LOC105378438 ; PLCE1
0.925 0.080 10 93993019 regulatory region variant T/G snv 0.21 3
rs12263737
PLCE1-AS1 ; PLCE1
1.000 0.080 10 94285156 intron variant G/A snv 0.32 2
rs11187870
NOC3L ; PLCE1
1.000 0.080 10 94328109 3 prime UTR variant G/C snv 6.3E-02 1
rs17109671
PLCE1
1.000 0.080 10 94031856 synonymous variant T/C snv 0.31 0.40 1
rs17417407
PLCE1
1.000 0.080 10 94171330 missense variant G/A;T snv 3.2E-05; 0.17 1
rs71031566
PLCE1-AS1 ; PLCE1
1.000 0.080 10 94287212 non coding transcript exon variant -/ATTT ins 0.29 1