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: rs9606756
rs9606756
TCN2
7 0.790 0.160 22 30610873 missense variant A/G snv 0.12 0.14 0.010 1.000 1 2015 2015