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: rs5029937
rs5029937
4 0.882 0.160 6 137874014 intron variant G/T snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs610604
rs610604
5 0.827 0.240 6 137878280 intron variant G/T snv 0.58 0.700 1.000 1 2011 2011