Gene: LINC01494 ×
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: rs188488867
rs188488867
LINC01494
1 2 218919534 intron variant C/T snv 2.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs77157375
rs77157375
LINC01494
1 2 218915189 intron variant G/A;C snv 0.700 1.000 1 2018 2018