Gene: LINC01470 ×
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: rs2910032
rs2910032
LINC01470
2 1.000 0.040 5 153160794 intron variant C/T snv 0.52 0.800 1.000 5 2013 2019
dbSNP: rs111294930
rs111294930
LINC01470
1 1.000 0.040 5 152797561 intron variant A/G snv 0.20 0.700 1.000 3 2014 2018
dbSNP: rs113568682
rs113568682
LINC01470
1 1.000 0.040 5 152920194 intron variant A/T snv 0.21 0.700 1.000 2 2017 2019
dbSNP: rs113897692
rs113897692
LINC01470
1 1.000 0.040 5 152797226 intron variant A/G snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs6868545
rs6868545
LINC01470
1 1.000 0.040 5 153115323 intron variant A/C snv 4.0E-02 0.700 1.000 1 2015 2015
dbSNP: rs72804786
rs72804786
LINC01470
1 1.000 0.040 5 152938239 intron variant G/A snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs7444191
rs7444191
LINC01470
2 1.000 0.040 5 152871873 intron variant G/A snv 0.54 0.700 1.000 1 2019 2019
dbSNP: rs76091702
rs76091702
LINC01470
1 1.000 0.040 5 153103403 intron variant C/A;T snv 3.9E-02 0.700 1.000 1 2017 2017