Gene: LINC02341 ×
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: rs11842146
rs11842146
LINC02341
1 13 42348370 intron variant C/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs1324003
rs1324003
LINC02341
1 13 42401990 intron variant C/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs180851
rs180851
LINC02341
1 13 42359904 intron variant C/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs7992415
rs7992415
LINC02341
1 13 42401161 intron variant A/C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs9533089
rs9533089
LINC02341
1 13 42376876 intron variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs9533093
rs9533093
LINC02341
1 13 42387461 intron variant T/C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs9533100
rs9533100
LINC02341
1 13 42422412 intron variant G/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs7998154
rs7998154
LINC02341
1 13 42349255 intron variant T/C snv 1.8E-02 0.700 1.000 1 2009 2009
dbSNP: rs7338012
rs7338012
LINC02341
1 13 42359990 intron variant A/C snv 5.9E-02 0.700 1.000 1 2009 2009
dbSNP: rs10507508
rs10507508
LINC02341
1 13 42395646 intron variant A/G snv 6.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs12854504
rs12854504
LINC02341
1 13 42409565 intron variant T/G snv 6.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs7987211
rs7987211
LINC02341
1 13 42392598 intron variant T/C snv 6.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs7987728
rs7987728
LINC02341
1 13 42392876 intron variant T/A;C snv 6.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs12873631
rs12873631
LINC02341
1 13 42394260 intron variant T/C snv 6.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs7994609
rs7994609
LINC02341
1 13 42394189 intron variant T/G snv 6.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs7994209
rs7994209
LINC02341
1 13 42393993 intron variant T/C snv 6.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs7992844
rs7992844
LINC02341
1 13 42394114 intron variant A/T snv 6.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs7994236
rs7994236
LINC02341
1 13 42394042 intron variant T/C snv 6.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs10507509
rs10507509
LINC02341
1 13 42398954 intron variant C/T snv 6.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs7989519
rs7989519
LINC02341
1 13 42397078 intron variant A/G snv 6.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs12874234
rs12874234
LINC02341
1 13 42396587 intron variant A/G snv 6.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs7993166
rs7993166
LINC02341
1 13 42394027 intron variant G/A snv 6.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs2875470
rs2875470
LINC02341
1 13 42399459 intron variant C/G snv 6.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs17638544
rs17638544
LINC02341
1 13 42382485 intron variant C/T snv 6.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs4454853
rs4454853
LINC02341
1 13 42399161 intron variant G/A snv 6.3E-02 0.700 1.000 1 2009 2009