rs1553173368, DVL1

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.
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2
CUI: C4225363
Disease: ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2
18 1.000 1 1337993 frameshift variant CGGTGCTGCCGCTGCC/- delins 0.700 0