rs104894043, SHH

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 3
CUI: C1840529
Disease: HOLOPROSENCEPHALY 3
37 0.925 0.120 7 155803613 missense variant C/T snv 4.4E-05 5.6E-05 0.800 1.000 12 1996 2009
Holoprosencephaly
CUI: C0079541
Disease: Holoprosencephaly
45 0.925 0.120 7 155803613 missense variant C/T snv 4.4E-05 5.6E-05 0.700 0