rs778148267, NFKB2

N. diseases: 1
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Malformations of Cortical Development, Group II
CUI: C1837249
Disease: Malformations of Cortical Development, Group II
101 1.000 0.080 10 102400738 missense variant G/A;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2017 2017