Gene: LINC01427 ×
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: rs10485630
rs10485630
LINC01427 ; LOC105372561
1 1.000 0.080 20 22265229 intron variant T/G snv 0.47 0.700 1.000 1 2012 2012
dbSNP: rs1569781
rs1569781
LINC01427
1 1.000 0.080 20 22281626 intron variant G/T snv 0.35 0.700 1.000 1 2012 2012
dbSNP: rs1569782
rs1569782
LINC01427
1 1.000 0.080 20 22281789 intron variant C/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs200366
rs200366
LINC01427
1 1.000 0.080 20 22279913 non coding transcript exon variant A/G snv 0.42 0.700 1.000 1 2012 2012
dbSNP: rs200369
rs200369
LINC01427
1 1.000 0.080 20 22284460 upstream gene variant A/C snv 0.37 0.700 1.000 1 2012 2012
dbSNP: rs2295099
rs2295099
LINC01427
1 1.000 0.080 20 22282494 non coding transcript exon variant G/A snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs4815101
rs4815101
LINC01427 ; LOC105372561
1 1.000 0.080 20 22274362 intron variant C/G snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs4815102
rs4815102
LINC01427 ; LOC105372561
1 1.000 0.080 20 22274535 non coding transcript exon variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs6047982
rs6047982
LINC01427 ; LOC105372561
2 1.000 0.080 20 22265812 intron variant T/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs6106493
rs6106493
LINC01427
1 1.000 0.080 20 22280255 non coding transcript exon variant C/T snv 0.35 0.700 1.000 1 2012 2012
dbSNP: rs6113604
rs6113604
LINC01427 ; LOC105372561
1 1.000 0.080 20 22271637 intron variant C/T snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs6113607
rs6113607
LINC01427 ; LOC105372561
1 1.000 0.080 20 22275632 intron variant T/C;G snv 0.700 1.000 1 2012 2012