Gene: LINC02551 ×
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: rs10791097
rs10791097
LINC02551
2 1.000 0.040 11 130848735 intron variant T/G snv 0.60 0.700 1.000 3 2014 2017
dbSNP: rs10750450
rs10750450
LINC02551
1 1.000 0.040 11 130849166 intron variant G/T snv 0.58 0.700 1.000 1 2019 2019
dbSNP: rs10791098
rs10791098
LINC02551
1 1.000 0.040 11 130848816 intron variant T/G snv 0.58 0.700 1.000 1 2019 2019