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: rs2952155
rs2952155
1 1.000 0.080 17 39705465 intron variant T/C;G snv 0.700 1.000 1 2011 2011