Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10816625
LOC105376214
0.925 0.080 9 108074792 regulatory region variant A/G snv 6.5E-02 1
rs10822013
ZNF365
0.851 0.080 10 62492218 intron variant C/T snv 0.42 2
rs10825036 0.882 0.080 10 53506471 intergenic variant T/G snv 0.21 1
rs10841753
SLCO1B1
0.925 0.080 12 21168436 intron variant T/C snv 0.19 1
rs10864459
PEX14
1.000 0.080 1 10503552 intron variant A/G;T snv 1
rs10871290 1.000 0.080 16 74438798 intron variant C/T snv 0.61 1
rs10885405
TCF7L2
1.000 0.080 10 113017911 intron variant C/T snv 0.53 1
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 2
rs10896449 0.827 0.200 11 69227200 intergenic variant A/G snv 0.53 3
rs10906522
FRMD4A
1.000 0.080 10 13865236 intron variant T/A;C snv 1
rs10906806
DCLRE1CP1 ; ACBD7-DCLRE1CP1
1.000 0.080 10 15029386 upstream gene variant T/C snv 0.41 1
rs10923574 1.000 0.080 1 118488075 regulatory region variant A/C;T snv 1
rs1092913
ROPN1L
0.925 0.080 5 10467590 intron variant G/A snv 0.19 1
rs10931936
CASP8
0.827 0.120 2 201279205 intron variant T/C snv 0.72 2
rs10941679 0.763 0.120 5 44706396 intergenic variant A/G snv 0.25 2
rs10995190
ZNF365
0.882 0.080 10 62518923 intron variant G/A snv 0.16 3
rs10995201
ZNF365
1.000 0.080 10 62540131 intron variant A/G snv 0.16 1
rs11075995
FTO
0.882 0.080 16 53821379 intron variant A/T snv 0.77 2
rs11076805
ADCY9
1.000 0.080 16 4056787 intron variant C/A;T snv 1
rs11082321
CABLES1
1.000 0.080 18 23196687 intron variant G/A snv 0.14 1
rs11096688 1.000 0.080 2 20885650 intergenic variant T/C snv 0.86 1
rs11117758
ESRRG
1.000 0.080 1 217047232 intron variant G/A snv 0.19 1
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 2
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21 17
rs111307654
PEG10 ; SGCE
1.000 0.080 7 94655777 intron variant -/AA;AAA;AAAA delins 1