Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4665972
SNX17
2 27375230 intron variant T/C snv 0.69 3
rs4849887 0.807 0.080 2 120487546 intergenic variant T/A;C snv 2
rs17356907
PGAM1P5
0.925 0.080 12 95633983 intron variant A/G snv 0.28 2
rs12173570 6 151636579 intergenic variant C/T snv 0.21 1
rs12371778 12 28003148 intergenic variant C/A;G snv 1
rs17625845 2 120332155 intergenic variant T/C snv 0.15 1
rs4820792 22 28765019 intergenic variant C/T snv 0.21 1
rs61280460 14 94329847 intergenic variant A/C;T snv 1
rs6557160 6 151628447 intergenic variant A/C snv 0.35 1
rs7816345 8 36988591 upstream gene variant C/T snv 0.26 1
rs62314947
LOC107986229
4 74577305 intron variant C/T snv 0.30 1
rs616402
PEX14
1 10506215 intron variant C/T snv 0.29 1
rs7089814
ZNF365
10 62427805 intron variant C/G;T snv 1