Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7200543
PDXDC1
16 15036113 synonymous variant A/G snv 0.35 0.30 6
rs2851682
FADS2
11 61848540 intron variant A/G snv 9.9E-02 5
rs11667159 19 46291989 intergenic variant C/A;T snv 3
rs11668290 19 46292921 upstream gene variant G/A snv 0.12 3
rs11671319 19 46291810 intergenic variant T/C snv 0.12 3
rs11671360 19 46291914 intergenic variant T/C snv 0.12 3
rs11671710 19 46288677 regulatory region variant C/G;T snv 3
rs117366905 19 46294033 upstream gene variant A/G snv 0.12 3
rs117992292 19 46294038 upstream gene variant A/G snv 0.12 3
rs141332218 19 46293976 upstream gene variant T/C snv 0.12 3
rs142815467 19 46291277 intergenic variant -/T delins 0.12 3
rs174536
TMEM258 ; MYRF
11 61784455 non coding transcript exon variant A/C snv 0.29 3
rs17764935
RAB3IL1
11 61897285 downstream gene variant G/A snv 4.9E-02 3
rs34128150 19 46291852 intergenic variant C/A snv 0.12 3
rs509360
MYRF ; TMEM258
11 61781087 intron variant A/G snv 0.61 0.52 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