Gene: LINC02660 ×
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: rs11252191
rs11252191
LINC02660
1 1.000 0.080 10 3921969 intron variant C/A;G;T snv 0.700 1.000 1 2014 2014
dbSNP: rs7086533
rs7086533
LINC02660
1 1.000 0.080 10 3926521 intron variant A/C snv 0.91 0.700 1.000 1 2014 2014