Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9303521
LINC02210-CRHR1
0.925 0.120 17 45727828 intron variant T/C;G snv 0.60 5
rs10108704 1.000 0.080 8 109350232 downstream gene variant G/T snv 0.17 2
rs16872704 1.000 0.080 6 12345461 intergenic variant A/G snv 0.22 2
rs7715147
ELOVL7
1.000 0.080 5 60757393 intron variant C/A;T snv 2
rs78523330
FBXO47
1.000 0.080 17 38949729 intron variant A/G snv 2.4E-02 2
rs4900006
LOC105370616 ; LOC105370617
1.000 0.080 14 89642343 intron variant C/A snv 5.2E-03 2