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: rs11121129
rs11121129
1 1.000 0.040 1 8208035 intron variant G/A snv 0.26 0.800 1.000 1 2012 2012
dbSNP: rs417065
rs417065
1 1.000 0.040 1 8204052 intron variant C/A snv 0.23 0.700 1.000 1 2015 2015