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: rs8141515
rs8141515
TCN2
1 1.000 0.160 22 30622085 intron variant T/C snv 0.11 0.700 1.000 1 2012 2012