Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2093210
rs2093210
C14orf39
1.000 0.040 14 60490561 intron variant C/T snv 0.45
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 5 2010 2019
dbSNP: rs33912345
rs33912345
SIX6 ; C14orf39
0.807 0.200 14 60509819 missense variant C/A;G snv 0.53
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019