Gene: LINGO2 ×
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: rs10968576
rs10968576
LINGO2
10 0.882 0.120 9 28414341 intron variant A/G snv 0.26 0.700 1.000 5 2010 2018
dbSNP: rs10968577
rs10968577
LINGO2
3 9 28415514 intron variant C/T snv 0.27 0.700 1.000 2 2015 2017
dbSNP: rs2183824
rs2183824
LINGO2
1 9 28412080 intron variant C/G;T snv 0.700 1.000 2 2017 2019
dbSNP: rs13299788
rs13299788
LINGO2
1 9 28941461 regulatory region variant C/G snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs1412239
rs1412239
LINGO2
4 0.925 0.120 9 28425517 intron variant C/G snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs16912921
rs16912921
LINGO2
1 9 28413463 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2183825
rs2183825
LINGO2
2 9 28412377 intron variant T/C snv 0.30 0.700 1.000 1 2019 2019