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: rs10945275
rs10945275
1 1.000 0.040 6 70958144 upstream gene variant C/T snv 0.23 0.010 1.000 1 2011 2011
dbSNP: rs2460691
rs2460691
1 1.000 0.040 6 70904152 intron variant G/C;T snv 0.010 1.000 1 2011 2011