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: rs764168489
rs764168489
CTNS ; LOC105371492
2 0.925 0.080 17 3656569 missense variant T/C snv 4.0E-06 0.700 1.000 9 1998 2012