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: rs1000778
rs1000778
3 1.000 0.040 11 61887833 intron variant A/G snv 0.59 0.700 1.000 1 2011 2011