Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121918598
RYR2
0.851 0.080 1 237648523 missense variant G/A;C snv 4
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs12362161 1.000 0.040 11 98834502 intergenic variant C/A;G snv 3
rs12369179
ZCCHC8
0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 16
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs1249958
PPP1R1A
0.925 0.040 12 54582053 missense variant C/T snv 2.7E-02 3
rs1253810269
ARID1A
0.882 0.080 1 26696971 missense variant G/A snv 7.0E-06 3
rs12564445
TNNT2
0.851 0.040 1 201376359 intron variant G/A snv 0.27 5
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs1258130495
EDNRA
0.882 0.040 4 147485727 missense variant G/A snv 3
rs12638540
CMTM7
1.000 0.040 3 32447042 intron variant A/G;T snv 1
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs13003941
ERBB4
0.925 0.040 2 211378978 3 prime UTR variant G/C;T snv 0.26 2
rs1303946678
CYP2D6 ; NDUFA6-DT
0.925 0.040 22 42126851 missense variant C/G snv 3
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs1320702652
MFAP1
0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1337916669
LOC108783645 ; HFE
0.925 0.040 6 26092879 missense variant G/T snv 2
rs139130723 1.000 0.040 6 14411553 intergenic variant A/G snv 4.4E-03 3
rs140226130
CCDC178
0.790 0.200 18 33336845 intron variant -/CTTTTTGCT delins 7.8E-02 8
rs142803096 1.000 0.040 6 14420151 intergenic variant G/C snv 4.4E-03 3
rs1429117513
LAG3
0.925 0.040 12 6775316 synonymous variant T/C snv 4.0E-06 2
rs144303414 1.000 0.040 18 48509413 intergenic variant A/C snv 1.5E-02 3
rs148133894 1.000 0.040 16 24584678 intergenic variant T/C snv 2.4E-03 3