Gene: LINC01221 ×
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: rs1036332
rs1036332
LINC01221
3 1 199043349 intron variant A/C snv 0.70 0.700 1.000 1 2012 2012
dbSNP: rs12125200
rs12125200
LINC01221
1 1 199022914 intron variant A/G snv 0.77 0.700 1.000 1 2012 2012
dbSNP: rs1434282
rs1434282
LINC01221
6 1 199041592 non coding transcript exon variant C/T snv 0.76 0.700 1.000 1 2012 2012
dbSNP: rs2360962
rs2360962
LINC01221
1 1 199035580 intron variant A/T snv 0.76 0.700 1.000 1 2012 2012
dbSNP: rs7529925
rs7529925
LINC01221
4 1 199038079 intron variant C/T snv 0.77 0.700 1.000 1 2012 2012