Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1285136498
NR3C1
0.807 0.080 5 143400101 missense variant G/A snv 13
rs1213469537
CAV1
0.882 0.080 7 116559145 missense variant C/T snv 4.0E-06 1.4E-05 9
rs796065354
ESR1
0.882 0.080 6 151944320 missense variant A/G snv 9
rs1131691036
TP53
0.851 0.080 17 7675207 frameshift variant GCA/CC delins 7
rs17822931
ABCC11
0.827 0.080 16 48224287 missense variant C/G;T snv 4.0E-06; 0.22 0.13 7
rs1800054
ATM
0.827 0.080 11 108227849 missense variant C/G;T snv 7.1E-03 7
rs3865014
GLCE
0.851 0.080 15 69269179 missense variant G/A snv 0.75 0.69 7
rs762292600
ESR1
0.925 0.080 6 151944316 missense variant A/G snv 4.0E-06 1.4E-05 7
rs769809364
TP73
0.807 0.080 1 3732940 missense variant G/A snv 8.5E-06 1.4E-05 7
rs13006529
CASP10
0.851 0.080 2 201217736 missense variant T/A snv 0.41 0.42 6
rs1453633223
CDKN2A
0.807 0.080 9 21974503 missense variant C/T snv 4.0E-06 6
rs188957694
ESR1
0.882 0.080 6 151944218 missense variant G/A;C snv 4.0E-05 4.9E-05 6
rs200863613
CDKN2A
0.925 0.080 9 21971061 missense variant C/A;T snv 8.5E-05 3.7E-04 6
rs3211371
CYP2B6
0.827 0.080 19 41016810 missense variant C/A;T snv 1.2E-04; 8.8E-02 6
rs372587282
KIDINS220
0.882 0.080 2 8733598 missense variant G/A;C snv 2.8E-05 6
rs4415084 0.827 0.080 5 44662413 upstream gene variant C/T snv 0.49 6
rs4778137
OCA2
0.827 0.080 15 28082689 intron variant C/A;G snv 6
rs4849887 0.807 0.080 2 120487546 intergenic variant T/A;C snv 6
rs660118
SART1
0.807 0.080 11 65967703 missense variant G/C snv 0.46 0.36 6
rs745542298
TP73
0.807 0.080 1 3732781 missense variant G/A;T snv 8.6E-06; 4.3E-06 2.1E-05 6
rs752295912
ERBB2
0.925 0.080 17 39710398 missense variant C/T snv 1.6E-05 6
rs759478535
ERBB2
0.851 0.080 17 39708351 missense variant A/G snv 6.8E-05 4.2E-05 6
rs11075995
FTO
0.882 0.080 16 53821379 intron variant A/T snv 0.77 5
rs11544331
C7orf50 ; GPER1
0.925 0.080 7 1091775 missense variant C/T snv 0.21 0.19 5
rs1408080623
PGR ; PGR-AS1
0.851 0.080 11 101128058 missense variant G/A snv 5