Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1260333
rs1260333 		12 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 0.700 1.000 1 2011 2011
dbSNP: rs579383
rs579383
MYRF ; TMEM258
2 11 61769111 intron variant G/A snv 0.58 0.700 1.000 1 2011 2011
dbSNP: rs174574
rs174574
FADS2
7 1.000 0.080 11 61832870 intron variant A/C snv 0.55 0.700 1.000 1 2011 2011
dbSNP: rs4713103
rs4713103
SYCP2L
1 6 10968908 intron variant G/T snv 0.55 0.700 1.000 1 2011 2011
dbSNP: rs2295602
rs2295602
ELOVL2
1 6 11005609 intron variant T/C snv 0.57 0.54 0.700 1.000 1 2011 2011
dbSNP: rs174449
rs174449 		2 11 61872907 downstream gene variant G/A snv 0.54 0.700 1.000 1 2011 2011
dbSNP: rs1570069
rs1570069
ELOVL2
1 6 11017592 intron variant A/G snv 0.54 0.700 1.000 1 2011 2011
dbSNP: rs7743830
rs7743830
ELOVL2
1 6 11013987 intron variant A/G snv 0.54 0.700 1.000 1 2011 2011
dbSNP: rs13966
rs13966
RAB3IL1
1 11 61897520 3 prime UTR variant T/C snv 0.53 0.700 1.000 1 2011 2011
dbSNP: rs6900220
rs6900220
ELOVL2-AS1
1 6 11064905 intron variant T/C snv 0.53 0.700 1.000 1 2011 2011
dbSNP: rs2147041
rs2147041
ELOVL2-AS1
1 6 11050290 intron variant A/G snv 0.53 0.700 1.000 1 2011 2011
dbSNP: rs3798707
rs3798707
ELOVL2
1 6 10991702 intron variant C/T snv 0.53 0.700 1.000 1 2011 2011
dbSNP: rs12587311
rs12587311 		1 14 28647489 intergenic variant T/C snv 0.53 0.700 1.000 1 2011 2011
dbSNP: rs3845427
rs3845427 		1 1 181293302 intergenic variant T/A snv 0.52 0.700 1.000 1 2011 2011
dbSNP: rs509360
rs509360
MYRF ; TMEM258
3 11 61781087 intron variant A/G snv 0.61 0.52 0.700 1.000 1 2011 2011
dbSNP: rs3798711
rs3798711
ELOVL2
1 6 11002577 intron variant T/C snv 0.52 0.700 1.000 1 2011 2011
dbSNP: rs1424760
rs1424760 		1 2 162925277 intergenic variant C/T snv 0.52 0.800 1.000 1 2012 2012
dbSNP: rs174616
rs174616
FADS2
3 1.000 0.080 11 61861650 intron variant G/A snv 0.51 0.700 1.000 1 2011 2011
dbSNP: rs8012543
rs8012543 		1 14 28618344 upstream gene variant G/A snv 0.50 0.700 1.000 1 2011 2011
dbSNP: rs7773173
rs7773173
SYCP2L
1 6 10956470 intron variant G/C snv 0.50 0.700 1.000 1 2011 2011
dbSNP: rs2391388
rs2391388
ALG14
2 1 95020269 intron variant A/C snv 0.49 0.700 1.000 1 2013 2013
dbSNP: rs174626
rs174626 		2 11 61869585 downstream gene variant G/A snv 0.48 0.700 1.000 1 2011 2011
dbSNP: rs102275
rs102275
TMEM258
18 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 0.800 1.000 3 2011 2013
dbSNP: rs198476
rs198476
MYRF ; MYRF-AS1
1 11 61758258 intron variant G/A snv 0.46 0.700 1.000 1 2011 2011
dbSNP: rs198462
rs198462
MYRF ; MYRF-AS1
1 11 61756647 intron variant G/A snv 0.46 0.700 1.000 1 2011 2011