Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35158985
CDH1
0.882 0.080 16 68762843 intron variant A/G snv 0.38 6
rs4778138
OCA2
0.851 0.080 15 28090674 intron variant A/G;T snv 6
rs10739221
LINC01505
0.851 0.080 9 106298549 intron variant T/C;G snv 5
rs251464
PPARGC1B
0.851 0.080 5 149816671 intron variant G/C snv 0.36 5
rs1636744
AHR
0.851 0.080 7 16944656 intron variant C/T snv 0.31 4
rs2995264
STN1
0.851 0.080 10 103909085 intron variant G/A snv 0.88 4
rs34466956
NFIC
0.882 0.080 19 3353624 intron variant C/T snv 0.49 4
rs498136 0.851 0.080 11 69552350 intergenic variant A/C snv 0.68 4
rs56238684
PIGU
0.882 0.080 20 34648892 intron variant G/C snv 4.2E-02 4
rs6750047
RMDN2
0.851 0.080 2 38049406 intron variant A/G snv 0.61 4
rs6914598
CDKAL1
0.851 0.080 6 21163688 intron variant T/C snv 0.38 4
rs10816595 0.851 0.080 9 107947454 regulatory region variant A/G snv 0.33 3
rs10830253
TYR
0.851 0.080 11 89294875 intron variant T/G snv 0.29 3
rs1148732
MIR614 ; GPRC5A
0.882 0.080 12 12915357 3 prime UTR variant G/A;C snv 3
rs11532907
MTAP
0.882 0.080 9 21844773 intron variant A/G;T snv 3
rs117648907
FMN1
0.882 0.080 15 32985509 intron variant C/T snv 1.4E-02 3
rs12596638
FTO
0.882 0.080 16 54081917 intron variant G/A snv 0.18 3
rs1484375
LINC01505
0.882 0.080 9 106305280 intron variant A/G;T snv 3
rs1640875
GPRC5A
0.882 0.080 12 12916590 3 prime UTR variant A/T snv 0.49 3
rs184628474
TTC7B
0.882 0.080 14 90719521 intron variant G/A snv 2.9E-02 3
rs186133190
WDPCP
0.882 0.080 2 63550724 intron variant T/C snv 4.9E-04 3
rs2005974
PLA2G6
0.882 0.080 22 38141105 non coding transcript exon variant G/A snv 0.49 3
rs2111398 0.882 0.080 12 12922268 downstream gene variant A/G snv 0.49 3
rs2290419
LOC338694
0.882 0.080 11 69152181 intron variant A/G snv 4.6E-02 3
rs2357176
SYNE2
0.882 0.080 14 63942595 intron variant G/A snv 0.68 3