Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs77960347
LIPG
18 49583585 missense variant A/C;G snv 4.0E-06; 8.7E-03 6
rs11046205
ABCC9
12 21839392 intron variant G/A snv 0.19 2
rs11265263 1 159740727 intergenic variant C/A;T snv 2
rs17689882
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
17 45829462 intron variant G/A snv 0.14 2
rs2175898
ESR1
6 151875817 intron variant C/G;T snv 2
rs228682
PER3
1 7796286 intron variant T/C snv 0.35 2
rs10473984
CRHBP
5 76971301 intron variant G/T snv 0.12 1
rs1080963 22 15376497 intergenic variant C/T snv 1
rs12137927
PER3
1 7811169 intron variant T/C snv 0.20 1
rs138191010 7 145416641 intergenic variant G/T snv 1
rs1403522266
GABRB1
4 47320137 missense variant A/G snv 4.0E-06 1
rs1475157 6 6016936 intergenic variant A/G snv 0.17 1
rs2965087
LOC101927870 ; RELN
7 103471538 intron variant T/C snv 0.45 1
rs3756290
RAPGEF6
5 131616057 intron variant A/G snv 0.56 1
rs4481363
LOC105377703
5 165047713 intron variant C/A snv 0.55 1
rs5440
GNB3 ; P3H3
12 6839735 3 prime UTR variant A/G snv 0.56 1
rs58682566
EPG5
18 45951902 intron variant A/G snv 9.9E-02 1
rs713224
F11-AS1
4 186491213 intron variant G/A;C snv 1
rs749865093
TPH1
11 18029360 missense variant C/T snv 3.2E-05 1
rs753009654
NRN1
6 6002360 missense variant C/A;T snv 4.0E-06 1
rs757522886
MTR
1 236885125 missense variant C/T snv 8.0E-06 1
rs7582472 2 133887223 regulatory region variant T/C snv 0.21 1
rs8836
ZACN ; EXOC7
17 76081416 3 prime UTR variant G/A;C;T snv 1.6E-05; 0.54; 4.8E-05 1
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 9
rs2239547
ITIH4
0.882 0.040 3 52821213 intron variant T/C snv 0.27 6