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: rs911196
rs911196
ELOVL2
1 6 10990518 intron variant T/G snv 0.18 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: 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: 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: rs953413
rs953413
ELOVL2
1 6 11012626 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs17606561
rs17606561
ELOVL2
2 1.000 0.040 6 10982126 3 prime UTR variant G/A snv 0.17 0.800 1.000 2 2011 2012
dbSNP: rs2236212
rs2236212
ELOVL2
2 1.000 0.040 6 10994782 intron variant G/C snv 0.39 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: rs8523
rs8523
ELOVL2
2 6 10980820 3 prime UTR variant G/A;C snv 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: 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: rs9393903
rs9393903
ELOVL2 ; ELOVL2-AS1
3 6 11042676 intron variant G/A snv 0.18 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