rs28933406, LRRC56;HRAS

N. diseases: 27
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.
NOONAN SYNDROME 3
CUI: C1860991
Disease: NOONAN SYNDROME 3
33 0.667 0.480 11 533875 missense variant G/C;T snv 0.700 0
Spermatocytic seminoma
CUI: C0334517
Disease: Spermatocytic seminoma
2 0.667 0.480 11 533875 missense variant G/C;T snv 0.700 0