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: rs6076920
rs6076920
1 1.000 0.080 20 6048671 intron variant C/G snv 9.8E-02 0.700 1.000 1 2007 2007