rs104894052, 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.
SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR
3 0.925 0.160 7 155803294 missense variant A/G snv 0.800 1.000 2 2001 2004
HOLOPROSENCEPHALY 3
CUI: C1840529
Disease: HOLOPROSENCEPHALY 3
37 0.925 0.160 7 155803294 missense variant A/G snv 0.700 1.000 12 1996 2009