Gene: LINC02444 ×
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: rs10785010
rs10785010
LINC02444
1 12 73157487 upstream gene variant T/A;C snv 0.700 1.000 1 2014 2014
dbSNP: rs10879572
rs10879572
LINC02444
1 12 73157791 upstream gene variant C/T snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs11179580
rs11179580
LINC02444
1 12 73192799 intron variant C/T snv 0.27 0.700 1.000 1 2014 2014
dbSNP: rs12811378
rs12811378
LINC02444
1 12 73160134 intron variant C/G snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs12813018
rs12813018
LINC02444
1 12 73160218 intron variant T/A snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs12826112
rs12826112
LINC02444
1 12 73162120 intron variant T/C snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs1976729
rs1976729
LINC02444
1 12 73159309 non coding transcript exon variant G/A;C;T snv 0.700 1.000 1 2014 2014
dbSNP: rs1976730
rs1976730
LINC02444
1 12 73159402 non coding transcript exon variant A/G snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs2176205
rs2176205
LINC02444
1 12 73159438 non coding transcript exon variant C/T snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs7299264
rs7299264
LINC02444
1 12 73159557 intron variant A/C;T snv 0.700 1.000 1 2014 2014
dbSNP: rs7302852
rs7302852
LINC02444
1 12 73163388 intron variant C/A snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs7960698
rs7960698
LINC02444
1 12 73158334 upstream gene variant C/G;T snv 0.700 1.000 1 2014 2014