rs121909067, TGIF1

N. diseases: 2
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.
HOLOPROSENCEPHALY 4 (disorder)
CUI: C1840528
Disease: HOLOPROSENCEPHALY 4 (disorder)
9 0.925 0.120 18 3456525 missense variant C/G snv 0.800 1.000 2 2000 2004
Holoprosencephaly
CUI: C0079541
Disease: Holoprosencephaly
45 0.925 0.120 18 3456525 missense variant C/G snv 0.010 1.000 1 2007 2007