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: 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: rs3798710
rs3798710
ELOVL2
1 6 11002550 intron variant G/C snv 0.18 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: rs9295757
rs9295757
ELOVL2
1 6 11033392 intron variant G/T 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: rs2180725
rs2180725
ELOVL2
1 6 11025187 intron variant T/C snv 0.17 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: rs3734398
rs3734398
ELOVL2
1 6 10982740 3 prime UTR variant T/C snv 0.41 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: rs3798711
rs3798711
ELOVL2
1 6 11002577 intron variant T/C snv 0.52 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: rs7744440
rs7744440
ELOVL2
1 6 11038278 intron variant T/G snv 0.39 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