Gene: CCDC39 ×
Source: CLINVAR ×
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: rs1560092440
rs1560092440
CCDC39
1 3 180660684 stop gained A/T snv 0.700 0
dbSNP: rs587778821
rs587778821
TTC14 ; CCDC39
1 3 180616873 frameshift variant TAC/A delins 0.700 0
dbSNP: rs769223754
rs769223754
CCDC39
1 3 180641993 missense variant C/A;T snv 7.0E-05; 4.3E-06 0.700 0
dbSNP: rs778577109
rs778577109
CCDC39
1 3 180661932 stop gained G/A snv 5.2E-06 7.0E-06 0.700 0
dbSNP: rs780175755
rs780175755
CCDC39
1 3 180659759 frameshift variant AG/- delins 1.6E-05 0.700 0
dbSNP: rs863224531
rs863224531
CCDC39
1 3 180644141 frameshift variant A/- del 0.700 0
dbSNP: rs878855279
rs878855279
CCDC39
1 3 180651492 frameshift variant TTGT/- delins 0.700 0
dbSNP: rs878855280
rs878855280
CCDC39
1 3 180663913 frameshift variant TA/- delins 0.700 0