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: rs1057518944
rs1057518944
NIPBL
9 0.807 0.280 5 36984990 frameshift variant CT/- delins 0.700 0
dbSNP: rs138119149
rs138119149
AARS2 ; TMEM151B
11 0.807 0.280 6 44304512 missense variant G/A snv 2.1E-04 2.4E-04 0.700 0
dbSNP: rs1553856553
rs1553856553
TP63
3 0.925 0.200 3 189864391 missense variant C/T snv 0.700 0
dbSNP: rs1565308384
rs1565308384
MYRF ; TMEM258
5 0.827 0.200 11 61784321 frameshift variant -/A delins 0.700 0
dbSNP: rs587777589
rs587777589
AARS2
7 0.851 0.280 6 44311095 frameshift variant -/C delins 0.700 0
dbSNP: rs771237928
rs771237928
NOTCH2
14 0.752 0.280 1 119915813 frameshift variant G/-;GG delins 0.700 0