Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11656696
GAS7
0.882 0.040 17 10130362 intron variant C/A snv 0.36 5
rs11710139
LOC107986142 ; LOC107986141
1.000 0.040 3 150341555 non coding transcript exon variant G/A snv 0.21 1
rs1210326005
LOXL1 ; LOXL1-AS1
1.000 0.040 15 73927510 missense variant C/G;T snv 1.2E-05 1
rs12150284
GAS7
1.000 0.040 17 10127773 intron variant C/A;G;T snv 3
rs12154178
ESR1
0.925 0.040 6 151929945 intron variant C/A snv 0.59 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121909193
MYOCOS ; MYOC
0.925 0.040 1 171636349 missense variant C/A snv 2
rs121909194
MYOC ; MYOCOS
0.882 0.040 1 171636302 missense variant C/G snv 3
rs121918071
TTR
0.882 0.240 18 31595209 missense variant C/A snv 4
rs12377624
LOC105376277
1.000 0.040 9 126610831 intron variant G/C snv 0.28 2
rs12377632
TLR4
0.827 0.120 9 117710452 intron variant T/A;C snv 5
rs12440667
LOXL1
1.000 0.040 15 73939098 intron variant C/A;T snv 2
rs1256031
ESR2
0.790 0.200 14 64279461 intron variant G/A;T snv 0.57 9
rs12699251
THSD7A
1.000 0.040 7 11639486 intron variant A/G snv 0.33 1
rs12913832
HERC2
0.763 0.200 15 28120472 intron variant A/G snv 0.50 15
rs12994401
LOC730100
0.925 0.040 2 51845108 intron variant C/T snv 0.18 2
rs13178997
WDR36
0.925 0.040 5 111108550 intron variant G/A;T snv 2
rs1401907822
B4GALT7
1.000 0.040 5 177608566 missense variant G/A snv 1
rs140967767
MYOCOS ; MYOC
0.925 0.040 1 171636106 missense variant G/A snv 1.9E-04 3.4E-04 2
rs1412829
CDKN2B-AS1
0.742 0.400 9 22043927 intron variant A/G snv 0.28 14
rs1437969513
FOXC1
1.000 0.040 6 1611203 missense variant C/T snv 1.1E-05 1
rs1438561194
WDR36
1.000 0.040 5 111092304 missense variant G/A snv 4.0E-06 7.0E-06 1
rs151326733
DERA
1.000 0.040 12 16036544 intron variant G/C snv 1.0E-02 1
rs1554200992
GJA1
0.925 0.160 6 121446966 missense variant C/T snv 2
rs1579050
FMNL2
0.925 0.040 2 152508013 intron variant A/G snv 0.42 3