Gene: LINC02694 ×
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: rs2624265
rs2624265
LINC02694
3 15 38856448 intron variant T/C snv 0.28 0.700 1.000 1 2009 2009
dbSNP: rs7176058
rs7176058
LINC02694 ; LOC105370780
1 15 39171966 intron variant A/G snv 0.26 0.700 1.000 1 2018 2018