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: rs17656349
rs17656349
2 1.000 0.040 5 150226431 intron variant C/T snv 0.45 0.700 1.000 1 2017 2017