NFIB, nuclear factor I B, 4781

N. diseases: 102; N. variants: 22
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: rs10810107
rs10810107
9 14195828 intron variant C/A;G snv
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs1328006
rs1328006
9 14516669 regulatory region variant C/T snv 0.45
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs4237133
rs4237133
9 14151961 intron variant C/A;G;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs7875078
rs7875078
9 14494847 intergenic variant C/A snv 0.54
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018