Gene: LINC01006 ×
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: rs2365286
rs2365286
LINC01006
1 7 156465485 intron variant G/A snv 0.67 0.700 1.000 1 2019 2019
dbSNP: rs6459680
rs6459680
LINC01006
2 7 156465874 intron variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs868822
rs868822
LINC01006
2 1.000 0.080 7 156460245 intron variant T/A;G snv 0.59 0.700 1.000 1 2019 2019