Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1007323
LOC101928191 ; SYCP2L
6 10953011 intron variant T/A;G snv 1
rs10792320 11 61978819 intergenic variant A/C;T snv 1
rs12199131
LOC101928191 ; SYCP2L
6 10932336 intron variant G/A;T snv 1
rs1225717
SYCP2L
6 10978007 intron variant A/G;T snv 1
rs12472274
ILKAP
2 238186781 non coding transcript exon variant G/A;T snv 1
rs12526913 6 11082691 downstream gene variant A/G;T snv 1
rs1321536
ELOVL2
6 11018579 intron variant T/A;G snv 1
rs1323739
ELOVL2
6 11004328 intron variant C/G;T snv 1
rs174589
FADS2
11 61848331 intron variant C/G;T snv 0.19 1
rs17764592
ELOVL2
6 11002911 intron variant A/C;G snv 1
rs198428
DAGLA
11 61722233 intron variant A/G;T snv 1
rs2028062 11 61978481 intergenic variant G/A;C snv 1
rs2235093
RAB3IL1
11 61897650 3 prime UTR variant A/G;T snv 1
rs2945816
OR8I2
11 56094615 downstream gene variant T/C snv 1
rs3117181
TNXB
6 32103240 intron variant C/A;G;T snv 1
rs3758977
LOC399900
11 61969772 upstream gene variant T/A;G snv 1
rs4532436
ELOVL2
6 10983738 3 prime UTR variant C/A;G;T snv 0.54; 5.0E-06 1
rs4711171
ELOVL2-AS1
6 11074114 intron variant C/A;T snv 1
rs4963444 11 62005870 regulatory region variant G/A;T snv 1
rs569258
MYRF-AS1 ; MYRF
11 61753196 intron variant T/C;G snv 1
rs6918936
SYCP2L
6 10959925 intron variant G/A;C snv 1
rs6920247
SYCP2L
6 10959940 intron variant C/A;G snv 1
rs7337573
LINC01442
13 60939535 intron variant T/C snv 1
rs7490068 13 103408045 intergenic variant G/A;C snv 1
rs7774711
SYCP2L
6 10964788 intron variant A/G;T snv 1