Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10818854
DENND1A
0.851 0.200 9 123684499 intron variant G/A snv 5.7E-02 6
rs10830962 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 7
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs10865238
FSHR
1.000 0.120 2 49041665 intron variant A/G snv 0.63 1
rs10876920
HSD17B6
1.000 0.120 12 56782391 intron variant C/G;T snv 0.50 1
rs10887800
LOC101929727 ; RNLS
0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs10986105
DENND1A
0.925 0.200 9 123787676 intron variant T/G snv 6.9E-02 2
rs10993397
AOPEP
1.000 0.120 9 94917489 intron variant C/T snv 0.33 1
rs11031005
LOC105376607
1.000 0.120 11 30204809 intron variant T/C snv 0.10 5
rs11031006
LOC105376607
0.882 0.120 11 30204981 intron variant G/A snv 0.11 8
rs11031010
LOC105376607
1.000 0.120 11 30218631 intron variant C/A snv 0.11 1
rs11039155
NR1H3
0.827 0.400 11 47259211 5 prime UTR variant G/A snv 0.14 0.12 6
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 10
rs11171718
SUOX ; RAB5B
1.000 0.120 12 55995838 3 prime UTR variant G/A snv 4.0E-02 1
rs11196218
TCF7L2
0.925 0.160 10 113080735 intron variant G/A snv 0.25 2
rs11196229
TCF7L2
0.925 0.160 10 113106413 intron variant G/A snv 0.19 2
rs11196236
TCF7L2
0.925 0.160 10 113127963 intron variant T/C snv 0.16 2
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs11212617
C11orf65
0.827 0.200 11 108412434 intron variant C/A snv 0.49 7
rs112137861
SOX5
1.000 0.120 12 23857104 intron variant C/A snv 3.3E-02 2
rs11225138
YAP1
0.925 0.200 11 102123167 intron variant G/C snv 6.1E-02 2
rs11225154
YAP1
1.000 0.120 11 102172509 intron variant G/A;C snv 1
rs11225161
YAP1
1.000 0.120 11 102199763 intron variant C/T snv 7.0E-02 1
rs1127760
FST
1.000 0.120 5 53484287 missense variant T/A snv 1
rs1127761
FST
1.000 0.120 5 53484289 stop gained T/A;C snv 2.8E-05 1