Gene: SNHG28 ×
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: rs6659742
rs6659742
SNHG28
1 1.000 0.080 1 159848723 intron variant C/T snv 0.39 0.800 1.000 1 2013 2013