Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs201921722 0.925 0.040 11 123679999 downstream gene variant -/A delins 9.2E-06 3
rs58598658
KLF12
0.925 0.080 13 73887725 intron variant -/A;AA delins 4
rs34177316
LOC107986273 ; APBB2
0.925 0.040 4 40985283 intron variant A/-;AA;AAA delins 3
rs528732638
CHST9 ; AQP4-AS1
0.851 0.120 18 26940224 intron variant A/-;AA;AAA;AAAA delins 2
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 15
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 10
rs11152369
TCF4
0.851 0.040 18 55399097 intron variant A/C snv 6.3E-02 5
rs17673138
NRG1
0.851 0.040 8 32840440 intron variant A/C snv 8.6E-02 4
rs2546057 1.000 0.040 19 33829949 intergenic variant A/C snv 0.41 3
rs11039409
NUP160
1.000 0.040 11 47814169 intron variant A/C snv 0.22 2
rs16854048
BEND4
1.000 0.040 4 42121711 intron variant A/C snv 0.23 2
rs184924771
LINC02699
1.000 0.040 11 25863658 intergenic variant A/C snv 1.2E-02 2
rs2286798
ITIH1
1.000 0.040 3 52787161 intron variant A/C snv 0.38 0.37 2
rs56403421 1.000 0.040 18 55098052 regulatory region variant A/C snv 0.26 2
rs600011
BBX
1.000 0.040 3 107576545 intron variant A/C snv 0.25 2
rs72788286
ATAD2B
1.000 0.040 2 23875451 intron variant A/C snv 0.12 2
rs7296288
DHH
0.851 0.080 12 49086185 upstream gene variant A/C snv 0.50 2
rs77607745 1.000 0.040 13 69001052 intergenic variant A/C snv 0.15 2
rs9972552
PGBD4
1.000 0.040 15 34104712 3 prime UTR variant A/C snv 0.99 2
rs1039197 1.000 0.040 10 4617005 intergenic variant A/C snv 0.71 1
rs10904299 1.000 0.040 10 4603975 intergenic variant A/C snv 0.21 1
rs11135349 1.000 0.040 5 165096466 intron variant A/C snv 0.61 1
rs12496634
PBRM1
1.000 0.040 3 52675243 intron variant A/C snv 0.34 1
rs12923444
METTL9
1.000 0.040 16 21628389 intron variant A/C snv 0.32 1
rs1343605 1.000 0.040 13 53072913 intergenic variant A/C snv 0.63 1