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: rs6113607
rs6113607
LINC01427 ; LOC105372561
1 1.000 0.080 20 22275632 intron variant T/C;G snv 0.700 1.000 1 2012 2012