Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10947055 6 30125587 intergenic variant T/C snv 0.11 2
rs16830359 1.000 0.080 1 43130713 intergenic variant G/A;T snv 2
rs1484170 10 80939735 downstream gene variant T/C snv 0.17 1
rs17636733 15 25667192 intergenic variant T/C snv 0.41 1
rs1916521 10 55657201 intergenic variant C/T snv 0.36 1
rs1320448
COL17A1
10 104086316 upstream gene variant A/G snv 0.92 1
rs12757165
ESRRG
1 216543195 intron variant A/G snv 0.29 1
rs152528
FGF1 ; SPRY4-AS1
5 142638295 intron variant C/T snv 0.28 1
rs12907914
LINC02694 ; LOC105370781
15 39023157 intron variant G/C snv 0.30 1
rs3729931
RAF1
3 12585017 intron variant G/A snv 0.35 0.43 1