Gene: LINC02718 ×
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: rs10833965
rs10833965
LINC02718
1 11 23193334 intron variant A/G snv 0.57 0.700 1.000 1 2017 2017
dbSNP: rs11602836
rs11602836
LINC02718
1 11 23211338 intergenic variant C/A;G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs11828289
rs11828289
LINC02718
1 11 23174695 intron variant G/C;T snv 0.700 1.000 1 2017 2017
dbSNP: rs16910800
rs16910800
LINC02718
1 11 23181239 intron variant C/T snv 0.20 0.700 1.000 1 2017 2017
dbSNP: rs17234274
rs17234274
LINC02718
1 11 23192820 intron variant A/C snv 0.40 0.700 1.000 1 2017 2017