rs137853235, HGF

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.
DEAFNESS, AUTOSOMAL RECESSIVE 39 (disorder)
CUI: C1842342
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 39 (disorder)
1 1.000 0.120 7 81752250 splice region variant C/T snv 4.0E-06 0.700 0