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: rs71636784
rs71636784
4 1.000 0.040 1 26842709 intron variant T/G snv 0.12 0.700 1.000 1 2019 2019