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: rs10518765
rs10518765
UNC13C
3 1.000 0.040 15 54388434 intron variant A/C snv 0.16 0.700 1.000 1 2006 2006