Gene: LINC01149 ×
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: rs2395004
rs2395004
LINC01149
1 6 31444736 intron variant G/C snv 0.41 0.700 1.000 1 2013 2013
dbSNP: rs2516467
rs2516467
LINC01149
1 6 31446021 non coding transcript exon variant T/C snv 6.8E-02 0.700 1.000 1 2013 2013
dbSNP: rs2524276
rs2524276
LINC01149
1 6 31440488 intron variant C/A snv 6.8E-02 0.700 1.000 1 2013 2013
dbSNP: rs2844510
rs2844510
LINC01149
1 6 31442631 intron variant G/T snv 0.11 0.700 1.000 1 2013 2013
dbSNP: rs2844520
rs2844520
LINC01149
1 6 31439981 intron variant G/T snv 6.8E-02 0.700 1.000 1 2013 2013