Gene: C14orf39 ×
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: rs2093210
rs2093210
C14orf39
4 1.000 0.040 14 60490561 intron variant C/T snv 0.45 0.700 1.000 5 2010 2019
dbSNP: rs33912345
rs33912345
SIX6 ; C14orf39
7 0.807 0.200 14 60509819 missense variant C/A;G snv 0.53 0.700 1.000 1 2019 2019