Gene: ELOVL2-AS1 ×
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: rs12662634
rs12662634
ELOVL2-AS1
1 6 11073958 intron variant G/A snv 0.17 0.700 1.000 1 2011 2011
dbSNP: rs1321535
rs1321535
ELOVL2-AS1
1 6 11075793 intron variant T/G snv 0.41 0.700 1.000 1 2011 2011
dbSNP: rs17675322
rs17675322
ELOVL2-AS1
1 6 11058952 intron variant T/A snv 0.59 0.700 1.000 1 2011 2011
dbSNP: rs17764682
rs17764682
ELOVL2-AS1
1 6 11058582 intron variant A/C snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs2147041
rs2147041
ELOVL2-AS1
1 6 11050290 intron variant A/G snv 0.53 0.700 1.000 1 2011 2011
dbSNP: rs4711170
rs4711170
ELOVL2-AS1
1 6 11070201 intron variant C/A snv 0.17 0.700 1.000 1 2011 2011
dbSNP: rs4711171
rs4711171
ELOVL2-AS1
1 6 11074114 intron variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs4713165
rs4713165
ELOVL2-AS1
1 6 11074069 intron variant T/C snv 0.41 0.700 1.000 1 2011 2011
dbSNP: rs6900220
rs6900220
ELOVL2-AS1
1 6 11064905 intron variant T/C snv 0.53 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: rs9368564
rs9368564
ELOVL2-AS1
1 6 11060050 intron variant A/G;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: rs9393915
rs9393915
ELOVL2-AS1
1 6 11072089 intron variant C/T snv 0.23 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