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: rs1018533
rs1018533
C14orf39
1 1.000 0.040 14 60504419 intron variant T/C snv 0.63 0.700 1.000 1 2012 2012
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 2016 2016