Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7947224
CNTN5
1.000 0.040 11 100002678 intron variant T/C snv 0.39 1
rs4684677
GHRLOS ; GHRL
0.742 0.360 3 10286769 missense variant T/A snv 0.10 6.6E-02 13
rs752298108
GHRL ; GHRLOS
1.000 0.040 3 10286806 missense variant C/T snv 4.0E-05 7.0E-06 1
rs696217
GHRL ; GHRLOS
0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs200312312
LOC105379109
1.000 0.040 5 104666645 intron variant T/C snv 0.16 1
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs1176744
HTR3B
0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs6589488
CADM1
1.000 0.040 11 115226236 intron variant A/T snv 0.90 1
rs4825476
GRIA3
0.925 0.040 X 123307628 intron variant G/A;C snv 2
rs117957029
LOC105370064
1.000 0.040 12 127200688 intron variant T/C snv 1.4E-02 1
rs2008387
MGMT
1.000 0.040 10 129650500 intron variant G/A snv 0.36 1
rs145241704 1.000 0.040 7 141805287 upstream gene variant T/G snv 7.4E-02 1
rs1285957 1.000 0.040 7 141889478 downstream gene variant T/C snv 0.86 1
rs33388
NR3C1
0.776 0.360 5 143317730 intron variant A/T snv 0.53 12
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31 23
rs10052957
NR3C1
0.851 0.160 5 143407136 non coding transcript exon variant G/A snv 0.28 4
rs200960801
ESR1
0.827 0.200 6 151944488 missense variant A/G snv 4.0E-06 6
rs726281
ESR1
1.000 0.040 6 151981443 intron variant G/A snv 0.56 1
rs3798577
ESR1
0.742 0.320 6 152099995 3 prime UTR variant T/C snv 0.45 16
rs2295193
SYNE1
1.000 0.040 6 152131959 intron variant G/A;C snv 1
rs929626
EBF1
0.925 0.120 5 158883623 intron variant A/G snv 0.40 2
rs495225
GHSR
0.882 0.040 3 172448243 synonymous variant G/A;C;T snv 0.66 4
rs9839776
SOX2-OT
0.851 0.160 3 181593779 intron variant C/G;T snv 4
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48