Gene: LINC01344 ×
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: rs1689800
rs1689800
LINC01344
2 1 182199750 intron variant A/G snv 0.34 0.800 1.000 2 2010 2013
dbSNP: rs1689788
rs1689788
LINC01344
3 1 182175287 intron variant T/C snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs1689797
rs1689797
LINC01344
1 1 182181843 intron variant C/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs2489279
rs2489279
LINC01344
1 1 182174984 intron variant C/A;G snv 0.700 1.000 1 2015 2015
dbSNP: rs61805076
rs61805076
LINC01344
1 1 182185855 intron variant T/C snv 0.26 0.700 1.000 1 2018 2018