Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17764935
RAB3IL1
11 61897285 downstream gene variant G/A snv 4.9E-02 3
rs2845573
FADS2
1.000 0.040 11 61834436 intron variant A/G snv 9.7E-02 3
rs34128150 19 46291852 intergenic variant C/A snv 0.12 3
rs498793
FADS2
1.000 0.040 11 61857233 intron variant T/C snv 0.62 3
rs509360
MYRF ; TMEM258
11 61781087 intron variant A/G snv 0.61 0.52 3
rs526126
FADS2
1.000 0.040 11 61857413 intron variant G/C;T snv 0.81; 8.0E-06 3
rs7254961 19 46292627 upstream gene variant C/T snv 0.12 3
rs7256047 19 46292776 upstream gene variant T/C snv 0.12 3
rs73059722 19 46293161 upstream gene variant G/A snv 0.12 3
rs73059723 19 46293245 upstream gene variant A/C snv 0.12 3
rs73059724 19 46293510 upstream gene variant T/C snv 0.11 3
rs73059725 19 46293511 upstream gene variant G/A snv 0.11 3
rs73059726 19 46293937 upstream gene variant G/A snv 0.12 3
rs80095739 19 46282441 regulatory region variant A/G snv 0.10 3
rs9393800
SYCP2L ; LOC101928191
6 10951504 intron variant A/G snv 0.20 3
rs9393903
ELOVL2 ; ELOVL2-AS1
6 11042676 intron variant G/A snv 0.18 3
rs10237735
PDE1C
7 32337136 intron variant C/T snv 7.6E-02 2
rs10414689 19 51293045 regulatory region variant T/C snv 0.11 2
rs10517480 4 59883111 intergenic variant A/T snv 0.27 2
rs1061808
PPT2 ; EGFL8 ; AGPAT1 ; PPT2-EGFL8
6 32168770 3 prime UTR variant T/G snv 0.64 2
rs10809457
LOC105375974
9 11402319 intron variant G/T snv 0.36 2
rs108499
TMEM258 ; MYRF
11 61779765 intron variant C/T snv 0.27 2
rs10885997
PNLIPRP2
10 116638460 synonymous variant A/G snv 0.38 0.36 2
rs1109748
LOC107984334 ; BEST1
11 61955173 synonymous variant C/A snv 0.21 0.11 2
rs11119805
LPGAT1
1 211744902 3 prime UTR variant T/A snv 0.13 2