Gene: LINC02438 ×
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: rs13101508
rs13101508
LINC02438
1 4 19275525 intron variant T/C snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs35177116
rs35177116
LINC02438
1 4 19338157 intron variant C/T snv 0.23 0.700 1.000 1 2018 2018