Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs1982073
TGFB1
0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs3087456
CIITA ; LOC105371080
0.742 0.480 16 10877045 intron variant G/A snv 0.53 14
rs1800012
COL1A1
0.763 0.320 17 50200388 intron variant C/A snv 0.14 13
rs1800544
ADRA2A
0.790 0.160 10 111076745 upstream gene variant G/C snv 0.59 12
rs3102735
COLEC10 ; TNFRSF11B
0.752 0.400 8 118952831 upstream gene variant T/C snv 0.17 12
rs3134069
COLEC10 ; TNFRSF11B
0.776 0.320 8 118952749 upstream gene variant A/C snv 9.6E-02 11
rs13182402
ALDH7A1
0.925 0.160 5 126582456 intron variant A/G snv 0.15 4
rs587777005
LGR4
0.925 0.120 11 27391119 stop gained G/A snv 1.4E-05 4
rs10085588
LOC105375412 ; SEM1 ; LOC105375411
1.000 0.080 7 96508362 intron variant A/G snv 0.72 3
rs1107748
LINC02594
1.000 0.080 17 43696446 intron variant T/C snv 0.54 3
rs3917
COL1A2
0.925 0.160 7 94431047 3 prime UTR variant -/GCTGTCC;GTTG;GTTGTCC;GTTGTGC ins 3
rs11898505
SPTBN1
2 54457420 intron variant A/G snv 0.76 2
rs1643821
ESR1
6 151862416 intron variant G/A snv 0.46 2
rs4342521
SEM1 ; LOC105375411
7 96506693 missense variant T/G snv 0.72 2
rs6469804
COLEC10
8 119032590 intron variant G/A;C snv 2
rs758488397
COL1A2
1.000 0.080 7 94412666 missense variant G/A;C snv 2
rs784288
MECOM
1.000 0.080 3 169253443 intron variant A/G;T snv 2
rs12475342
SPTBN1
2 54655541 intron variant G/A snv 0.28 1
rs17790156
LRP4
11 46883767 intron variant A/T snv 8.9E-02 1
rs270611
PDLIM4 ; P4HA2
5 132256377 intron variant C/A;T snv 1
rs2941584
SPTBN1
2 54654484 intron variant T/C snv 0.64 1
rs366512
P4HA2 ; PDLIM4
5 132258479 intron variant C/T snv 1.8E-02 1
rs3900945
P4HA2 ; PDLIM4
5 132257177 intron variant T/A;C snv 1
rs7570532
C2orf88 ; MSTN
2 190058686 intron variant A/G snv 0.34 1