Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs9400271
CCDC162P
6 109286353 non coding transcript exon variant G/A snv 0.51 5
rs11966072
CCDC162P
6 109313625 intron variant A/G snv 0.26 4
rs9400273
CCDC162P
6 109311596 intron variant A/G snv 0.40 2
rs13191948
CCDC162P
6 109313396 intron variant C/T snv 0.40 2
rs6568571
CCDC162P
6 109292049 intron variant A/C;T snv 2
rs9372208
CCDC162P
1.000 0.040 6 109274965 intron variant A/G;T snv 2
rs36052053
CCDC162P
6 109262596 intron variant G/A snv 0.11 2
rs6568570
CCDC162P
6 109292038 intron variant T/A;C;G snv 2
rs9480924
CCDC162P
6 109295867 intron variant T/C snv 0.40 2
rs200980971
CCDC162P
6 109261139 intron variant A/-;AA delins 2
rs12529733
CCDC162P
6 109332929 intron variant T/C snv 0.54 1
rs1546723
CCDC162P
6 109304676 intron variant G/A snv 0.40 1
rs6925716
CCDC162P
6 109276438 intron variant T/C snv 0.61 1
rs13210693
CCDC162P
1.000 0.040 6 109277761 intron variant G/A snv 0.61 1
rs9320282
CCDC162P
6 109298174 intron variant A/G snv 0.63 1
rs932223
CCDC162P
6 109265453 intron variant T/C snv 0.51 1
rs9487051
CCDC162P
6 109295876 intron variant A/G snv 0.41 1
rs9374081
CCDC162P
6 109310579 intron variant A/G snv 0.26 1
rs884366
CCDC162P
6 109252892 intron variant G/A snv 0.25 1
rs35424364
CCDC162P
1.000 0.080 6 109322402 intron variant -/T delins 1
rs9374080
CCDC162P
6 109295217 intron variant T/C snv 0.40 1
rs117368522
CCDC162P
6 109255740 intron variant G/A snv 5.0E-04 1
rs185030778
CCDC162P
6 109277348 intron variant C/T snv 6.3E-03 1
rs9386780
CCDC162P
6 109263207 intron variant A/G snv 0.63 1