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: rs3798723
rs3798723
ELOVL2
1 6 11041487 intron variant G/A snv 0.30 0.700 1.000 1 2011 2011
dbSNP: rs4532436
rs4532436
ELOVL2
1 6 10983738 3 prime UTR variant C/A;G;T snv 0.54; 5.0E-06 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: rs7743830
rs7743830
ELOVL2
1 6 11013987 intron variant A/G snv 0.54 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: rs8523
rs8523
ELOVL2
2 6 10980820 3 prime UTR variant G/A;C snv 0.700 1.000 1 2011 2011
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: 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: rs953413
rs953413
ELOVL2
1 6 11012626 intron variant G/A;C snv 0.700 1.000 1 2011 2011