Gene: LINC01122 ×
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: rs4671328
rs4671328
LINC01122
1 2 58708147 intron variant T/G snv 0.56 0.700 1.000 4 2017 2019
dbSNP: rs2075171
rs2075171
LINC01122
2 2 58461772 splice region variant G/A snv 0.18 0.700 1.000 2 2017 2018
dbSNP: rs929641
rs929641
LINC01122
3 2 58565242 intron variant A/G snv 0.45 0.700 1.000 2 2015 2018
dbSNP: rs10197655
rs10197655
LINC01122
1 2 58564285 intron variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs13011109
rs13011109
LINC01122
1 2 58630284 intron variant G/C snv 0.39 0.700 1.000 1 2015 2015
dbSNP: rs1641155
rs1641155
LINC01122
1 2 58738076 intron variant T/G snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs1861412
rs1861412
LINC01122
1 2 58665930 intron variant G/A snv 0.48 0.700 1.000 1 2019 2019
dbSNP: rs7573672
rs7573672
LINC01122
1 2 58927970 intron variant G/A;T snv 0.700 1.000 1 2019 2019