Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs886037845
TOR1AIP1
1 179917932 missense variant A/C snv 1
rs2232228
HAS3
16 69109674 synonymous variant A/C;G snv 8.1E-06; 0.40 1
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs11541796
TTR
0.807 0.280 18 31593011 missense variant A/G snv 9
rs869320740
TTN-AS1 ; TTN
0.851 0.200 2 178546102 missense variant A/G snv 4.1E-06 5
rs1799822
CPT2
0.925 0.080 1 53213557 missense variant A/G snv 0.16 0.15 4
rs267606782
EMD
0.925 0.120 X 154379485 start lost A/G snv 4
rs397516269
MYH7
0.882 0.080 14 23431426 missense variant A/G snv 4.0E-06 4
rs121912560
MYO6
0.925 0.160 6 75841299 missense variant A/G snv 4.0E-06 3
rs397516028
MYBPC3
1.000 0.080 11 47332594 missense variant A/G snv 3
rs121918070
TTR
1.000 0.120 18 31595157 missense variant A/G snv 4.0E-06 1.4E-05 2
rs1334828551
MUL1
1 20500800 missense variant A/G snv 4.0E-06 1.4E-05 2
rs267606976
PRKAG2
1.000 0.080 7 151564203 missense variant A/G snv 2
rs869312054
TTN ; TTN-AS1
2 178593566 splice donor variant A/G snv 1.4E-05 2
rs193922712
MYLK2
20 31821560 missense variant A/G snv 6.0E-05 5.6E-05 1
rs57045855
LMNA
0.882 0.040 1 156134464 missense variant A/G;T snv 6
rs786205436
SDHD
0.882 0.080 11 112088972 missense variant A/G;T snv 5
rs2043055
IL18
0.925 0.080 11 112160901 intron variant A/G;T snv 3
rs886042961
GAA
1.000 0.120 17 80108713 missense variant A/G;T snv 2
rs1800730
HFE ; LOC108783645
0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs267607123
TNNC1
0.882 0.080 3 52452222 missense variant A/T snv 4.0E-06 7.0E-06 4
rs397517735
TTN ; TTN-AS1
0.925 0.160 2 178559309 splice donor variant A/T snv 4.4E-06 4.9E-05 4
rs1057518905
DPM3
1 155140104 missense variant A/T snv 3
rs1568346416
UQCRFS1 ; LOC105372352
1.000 0.080 19 29213078 missense variant A/T snv 3