Gene: LINC00461 ×
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: rs10514301
rs10514301
LINC00461
2 5 88643836 intron variant C/T snv 0.16 0.700 1.000 3 2018 2019
dbSNP: rs6882046
rs6882046
LINC00461
2 1.000 0.040 5 88673046 non coding transcript exon variant A/G snv 0.29 0.700 1.000 3 2018 2019
dbSNP: rs10061788
rs10061788
LINC00461
2 1.000 0.040 5 88638889 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10070734
rs10070734
LINC00461
1 5 88644208 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs35267052
rs35267052
LINC00461
1 5 88653300 intron variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs3814424
rs3814424
LINC00461
1 5 88673135 non coding transcript exon variant C/T snv 0.21 0.700 1.000 1 2019 2019