Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34670419
ZKSCAN5
1.000 0.080 7 99533211 3 prime UTR variant G/A;T snv 7.7E-06; 2.6E-02 7
rs148982377
ZNF789 ; ZNF394
7 99477415 intron variant T/C snv 3.2E-02 4
rs10278040 7 99543750 downstream gene variant G/A snv 0.16 2
rs78900934 1.000 0.080 1 101272565 upstream gene variant C/A snv 0.32 2
rs2911280
CMIP
1.000 0.080 16 81557708 intron variant A/G snv 0.82 2
rs13222543
ZCWPW1
7 100417834 intron variant C/T snv 1.2E-02 2
rs111730697 13 21743520 intergenic variant TCCATCCATCCA/-;TCCA;TCCATCCA;TCCATCCATCCATCCA;TCCATCCATCCATCCATCCA;TCCATCCATCCATCCATCCATCCA;TCCATCCATCCATCCATCCATCCATCCA;TCCATCCATCCATCCATCCATCCATCCATCCA delins 1
rs143524414 7 99367992 intron variant G/A snv 5.3E-02 1
rs200943612 19 47909197 intergenic variant T/C snv 1
rs615567 13 21745070 intergenic variant A/T snv 0.39 1
rs67836407 13 21717951 TF binding site variant AGGTT/- delins 0.58 1
rs955783 13 21724936 intergenic variant A/T snv 0.37 1
rs150507409
ARPC1B
7 99386080 intron variant G/A snv 3.3E-02 1
rs77356530
ATP5MF-PTCD1 ; PTCD1
7 99421942 intron variant G/A snv 1.0E-02 1
rs57159061
CMIP
16 81557357 intron variant T/C snv 0.11 1
rs80193476
CYP3A43
7 99835967 intron variant A/G;T snv 2.8E-02 1
rs8042456
EIF2AK4
15 39998275 intron variant G/T snv 0.67 1
rs117430166
LOC107986828 ; CASTOR3
7 100229908 intron variant C/T snv 3.3E-02 1
rs36139342
MCM9
6 118883460 intron variant -/C delins 1
rs34022779
PTCD1 ; CPSF4 ; ATP5MF-PTCD1
7 99441691 intron variant T/-;TT;TTT delins 1
rs5935876
PUDP
X 7004037 intron variant G/A snv 0.34 1
rs28620926
SRP14-AS1
15 40064970 intron variant A/G snv 0.32 1
rs2431830
SULT2A1
19 47876949 intron variant C/G;T snv 1
rs296360
SULT2A1
19 47885401 intron variant T/C snv 0.12 1
rs77533229
THADA
2 43252499 intron variant G/A snv 1.8E-02 1