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: rs2103816
rs2103816
1 1.000 0.040 6 170366925 intron variant T/A snv 0.58 0.010 1.000 1 2012 2012
dbSNP: rs9460106
rs9460106
1 1.000 0.040 6 170306872 intron variant T/C;G snv 0.010 1.000 1 2012 2012