ELOVL2, ELOVL fatty acid elongase 2, 54898

N. diseases: 26; N. variants: 41
Disease: Phospholipid measurement ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs8523
rs8523 		6 10980820 3 prime UTR variant G/A;C snv
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs17606561
rs17606561 		1.000 0.040 6 10982126 3 prime UTR variant G/A snv 0.17
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.800 1.000 2 2011 2012
dbSNP: rs1225737
rs1225737 		6 10982419 3 prime UTR variant C/T snv 0.59
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs3734398
rs3734398 		6 10982740 3 prime UTR variant T/C snv 0.41
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs4532436
rs4532436 		6 10983738 3 prime UTR variant C/A;G;T snv 0.54; 5.0E-06
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs12195587
rs12195587 		6 10989709 synonymous variant G/A snv 0.12 0.11
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs2281591
rs2281591 		6 10990260 intron variant A/G snv 0.30
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs911196
rs911196 		6 10990518 intron variant T/G snv 0.18
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs3798707
rs3798707 		6 10991702 intron variant C/T snv 0.53
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs2236212
rs2236212 		1.000 0.040 6 10994782 intron variant G/C snv 0.39
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs3798709
rs3798709 		6 11001043 intron variant A/G snv 0.18
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs3798710
rs3798710 		6 11002550 intron variant G/C snv 0.18
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs3798711
rs3798711 		6 11002577 intron variant T/C snv 0.52
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs17764592
rs17764592 		6 11002911 intron variant A/C;G snv
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs1323739
rs1323739 		6 11004328 intron variant C/G;T snv
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs2295601
rs2295601 		6 11005453 synonymous variant G/A snv 0.22 0.21
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs2295602
rs2295602 		6 11005609 intron variant T/C snv 0.57 0.54
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs3798713
rs3798713 		6 11008389 intron variant G/C snv 0.41
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs17675073
rs17675073 		6 11008416 intron variant G/A snv 0.11
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs953413
rs953413 		6 11012626 intron variant G/A;C snv
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs7743830
rs7743830 		6 11013987 intron variant A/G snv 0.54
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs1570069
rs1570069 		6 11017592 intron variant A/G snv 0.54
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs1321536
rs1321536 		6 11018579 intron variant T/A;G snv
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs3756963
rs3756963 		0.882 0.200 6 11021921 intron variant T/C snv 0.24
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs2180725
rs2180725 		6 11025187 intron variant T/C snv 0.17
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011