Gene: ELOVL2 ×
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: rs9295764
rs9295764
ELOVL2 ; ELOVL2-AS1
1 6 11044963 non coding transcript exon variant A/G snv 0.59 0.700 1.000 1 2011 2011
dbSNP: rs9295763
rs9295763
ELOVL2 ; ELOVL2-AS1
1 6 11044959 non coding transcript exon variant G/A;C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs9393903
rs9393903
ELOVL2 ; ELOVL2-AS1
3 6 11042676 intron variant G/A snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs9468304
rs9468304
ELOVL2 ; ELOVL2-AS1
2 1.000 0.040 6 11041932 intron variant G/A snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs3798723
rs3798723
ELOVL2
1 6 11041487 intron variant G/A snv 0.30 0.700 1.000 1 2011 2011
dbSNP: rs3798722
rs3798722
ELOVL2
2 6 11040190 intron variant A/G snv 0.39 0.700 1.000 1 2011 2011
dbSNP: rs3798721
rs3798721
ELOVL2
1 6 11039950 intron variant A/C snv 0.31 0.700 1.000 1 2011 2011
dbSNP: rs7744440
rs7744440
ELOVL2
1 6 11038278 intron variant T/G snv 0.39 0.700 1.000 1 2011 2011
dbSNP: rs3798719
rs3798719
ELOVL2
1 6 11036592 intron variant C/T snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs6936315
rs6936315
ELOVL2
1 6 11035739 intron variant T/C snv 0.30 0.700 1.000 1 2011 2011
dbSNP: rs9295757
rs9295757
ELOVL2
1 6 11033392 intron variant G/T snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs3778166
rs3778166
ELOVL2
1 6 11032931 intron variant G/A snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs10498676
rs10498676
ELOVL2
3 0.925 0.040 6 11026766 intron variant G/A snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs2180725
rs2180725
ELOVL2
1 6 11025187 intron variant T/C snv 0.17 0.700 1.000 1 2011 2011
dbSNP: rs3756963
rs3756963
ELOVL2
4 0.882 0.200 6 11021921 intron variant T/C snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs1321536
rs1321536
ELOVL2
1 6 11018579 intron variant T/A;G snv 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: rs953413
rs953413
ELOVL2
1 6 11012626 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs17675073
rs17675073
ELOVL2
1 6 11008416 intron variant G/A snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs3798713
rs3798713
ELOVL2
1 6 11008389 intron variant G/C snv 0.41 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: rs2295601
rs2295601
ELOVL2
1 6 11005453 synonymous variant G/A snv 0.22 0.21 0.700 1.000 1 2011 2011
dbSNP: rs1323739
rs1323739
ELOVL2
1 6 11004328 intron variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs17764592
rs17764592
ELOVL2
1 6 11002911 intron variant A/C;G snv 0.700 1.000 1 2011 2011