NFIX, nuclear factor I X, 4784

N. diseases: 183; N. variants: 33
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1555696625
rs1555696625
0.851 0.360 19 13025409 missense variant G/A snv
CUI: C1837260
Disease: Prominent forehead
Prominent forehead
0.700 0
dbSNP: rs1568269273
rs1568269273
0.807 0.320 19 13025433 missense variant G/A snv
CUI: C1837260
Disease: Prominent forehead
Prominent forehead
0.700 0