Gene: LINC01505 ×
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: rs34575265
rs34575265
LINC01505
1 9 106181520 intron variant C/T snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs80311040
rs80311040
LINC01505
1 9 106701525 intron variant C/T snv 1.0E-04 0.700 1.000 1 2019 2019
dbSNP: rs902144
rs902144
LINC01505
1 9 106415290 intron variant G/C snv 0.53 0.700 1.000 1 2019 2019