Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs61348633
rs61348633
KRT5
2 0.925 0.080 12 52516652 missense variant T/C snv 0.010 1.000 1 2019 2019