Gene: LINC02652 ×
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: rs2807743
rs2807743
LINC02652
2 10 28491364 intron variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs2998286
rs2998286
LINC02652
5 10 28491444 intron variant T/C snv 0.73 0.700 1.000 1 2019 2019