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: rs9899183
rs9899183
TNFSF12 ; TNFSF12-TNFSF13
3 1.000 0.080 17 7549660 intron variant C/G;T snv 0.700 1.000 1 2018 2018