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: rs7338012
rs7338012
LINC02341
1 13 42359990 intron variant A/C snv 5.9E-02 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: rs7992970
rs7992970
LINC02341
1 13 42371327 intron variant A/G snv 0.26 0.700 1.000 2 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: rs11840862
rs11840862
LINC02341
1 13 42382327 intron variant A/G snv 0.56 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: rs1475249
rs1475249
LINC02341
1 13 42380369 intron variant A/G snv 0.26 0.700 1.000 1 2009 2009
dbSNP: rs238256
rs238256
LINC02341
1 13 42349539 intron variant A/G snv 0.37 0.700 1.000 1 2009 2009
dbSNP: rs417768
rs417768
LINC02341
1 13 42346262 intron variant A/G snv 0.38 0.700 1.000 1 2009 2009
dbSNP: rs7326472
rs7326472
LINC02341
1 13 42405815 intron variant A/G snv 1.0E-01 0.700 1.000 1 2009 2009
dbSNP: rs7327510
rs7327510
LINC02341
1 13 42414788 intron variant A/G snv 0.54 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: rs7992844
rs7992844
LINC02341
1 13 42394114 intron variant A/T snv 6.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs238252
rs238252
LINC02341
1 13 42341518 intron variant C/G snv 0.17 0.700 1.000 1 2009 2009
dbSNP: rs238257
rs238257
LINC02341
1 13 42350747 intron variant C/G snv 0.57 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: 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: rs9533090
rs9533090
LINC02341
3 13 42377313 intron variant C/T snv 0.39 0.800 1.000 4 2009 2018
dbSNP: rs9594738
rs9594738
LINC02341
1 13 42378009 intron variant C/T snv 0.39 0.800 1.000 3 2008 2018
dbSNP: rs9594759
rs9594759
LINC02341
1 13 42458457 intron variant C/T snv 0.51 0.800 1.000 3 2008 2009
dbSNP: rs8001611
rs8001611
LINC02341
2 13 42391558 intron variant C/T snv 0.59 0.700 1.000 2 2013 2018
dbSNP: rs10507509
rs10507509
LINC02341
1 13 42398954 intron variant C/T snv 6.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs17063206
rs17063206
LINC02341
1 13 42343323 intron variant C/T snv 0.16 0.700 1.000 1 2009 2009