rs199476091, PTCH1

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.
HOLOPROSENCEPHALY 7
CUI: C1835820
Disease: HOLOPROSENCEPHALY 7
7 1.000 0.120 9 95479038 missense variant C/T snv 4.2E-04 9.1E-05 0.700 1.000 3 2002 2006