rs672601361, TWNK

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.
PERRAULT SYNDROME 5
CUI: C4015307
Disease: PERRAULT SYNDROME 5
6 1.000 10 100989721 missense variant T/G snv 4.0E-06; 8.0E-06 1.4E-05 0.800 1.000 1 2014 2014