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: rs6012536
rs6012536
1 1.000 0.120 20 48807026 intron variant A/G snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs6095302
rs6095302
1 1.000 0.120 20 48813028 intron variant C/T snv 0.10 0.700 1.000 1 2011 2011