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: rs11759064
rs11759064
1 1.000 0.080 6 162379633 intron variant C/T snv 0.22 0.700 1.000 1 2017 2017