Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs201941147
ESR1
6 151735234 intron variant -/A ins 1
rs1366594
MEF2C-AS1
5 89080244 intron variant A/C snv 0.57 3
rs227584
HROB
17 44148179 missense variant A/C snv 0.40 0.48 2
rs4817775
LOC100133286
21 36112764 intron variant A/C snv 0.49 2
rs6557160 6 151628447 intergenic variant A/C snv 0.35 2
rs1036066
GNG12-AS1 ; WLS
1 68194522 intron variant A/C snv 0.33 1
rs10490046
SLC8A1
2 40403538 intron variant A/C snv 0.28 1
rs1159798
LNCAROD ; LOC105378305
10 52652733 intron variant A/C snv 0.70 1
rs273573
DCDC1 ; LOC105376611
11 30889444 intron variant A/C snv 0.69 1
rs2982554
ESR1
6 151736875 intron variant A/C snv 0.49 1
rs3020307
ESR1
6 151746109 intron variant A/C snv 0.45 1
rs3103995
LOC105375723 ; SAMD12-AS1
8 118860712 intron variant A/C snv 0.41 1
rs4335155
COLEC10
8 119001230 intron variant A/C snv 0.59 1
rs4354338
COLEC10
8 119003821 intron variant A/C snv 0.65 1
rs59412811
SMIM29
6 34250798 intron variant A/C snv 0.17 1
rs7338012
LINC02341
13 42359990 intron variant A/C snv 5.9E-02 1
rs73403830
ANKS1A
6 35038899 intron variant A/C snv 4.8E-02 1
rs73719807 7 121551197 intergenic variant A/C snv 0.13 1
rs74394007
LEKR1
3 156974418 intron variant A/C snv 0.17 1
rs7741021
RSPO3
6 127147129 intron variant A/C snv 0.42 1
rs921874
FZD4-DT ; LOC105369422
11 87012962 intron variant A/C snv 0.74 1
rs10226308
EPDR1 ; NME8
7 37898820 intron variant A/C;G snv 2
rs3801387
WNT16
7 121334711 intron variant A/C;G snv 2
rs12901789
IQCH
15 67269876 intron variant A/C;G snv 1
rs1471399 4 87852921 regulatory region variant A/C;G snv 1