Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6088343 1.000 0.040 20 33908259 downstream gene variant C/T snv 0.46 3
rs11264339 1.000 0.040 1 155168172 downstream gene variant C/T snv 0.56 2
rs11265022 1.000 0.040 1 158542829 downstream gene variant T/A snv 0.21 2
rs13220395 1.000 0.040 6 26055140 downstream gene variant G/A;C snv 2
rs2726034 1.000 0.040 16 28325561 downstream gene variant T/C snv 0.37 2
rs10057744
FOXI1
1.000 0.040 5 170109750 downstream gene variant C/T snv 0.89 1
rs10117202
LOC107987053
1.000 0.040 9 21323090 downstream gene variant T/A;G snv 1
rs10117872 1.000 0.040 9 4888355 downstream gene variant C/T snv 9.7E-02 1
rs1018144 1.000 0.040 8 106219142 downstream gene variant G/A snv 0.58 1
rs10186957 1.000 0.040 2 206622165 downstream gene variant C/T snv 0.86 1
rs10204358 1.000 0.040 2 53466481 downstream gene variant T/C snv 6.2E-02 1
rs10458204
LOC105374904
1.000 0.040 6 6996246 downstream gene variant T/C snv 0.12 1
rs10492690
STOML3
1.000 0.040 13 38965827 downstream gene variant C/T snv 0.19 1
rs10492692 1.000 0.040 13 38962460 downstream gene variant G/A;C snv 1
rs10507041 1.000 0.040 12 94550919 downstream gene variant G/A snv 0.21 1
rs10739569 1.000 0.040 9 120598749 downstream gene variant G/A;C snv 1
rs10740667 1.000 0.040 10 56368030 downstream gene variant A/G snv 0.68 1
rs1076534
MYBPC1
1.000 0.040 12 101686733 downstream gene variant C/T snv 1.6E-02 1
rs10772679 1.000 0.040 12 7726004 downstream gene variant G/T snv 0.86 1
rs10778139
MYBPC1
1.000 0.040 12 101689424 downstream gene variant A/C;G snv 1
rs10817367 1.000 0.040 9 112671884 downstream gene variant G/A snv 0.29 1
rs10828003 1.000 0.040 10 20291196 downstream gene variant T/G snv 0.28 1
rs10830359 1.000 0.040 11 89722276 downstream gene variant T/A;C snv 0.30 1
rs10915342 1.000 0.040 1 5086011 downstream gene variant T/C snv 0.20 1
rs10950819 1.000 0.040 7 20594113 downstream gene variant G/A snv 0.35 1