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: rs7934094
rs7934094
1 11 43484157 intron variant T/G snv 0.15 0.700 1.000 2 2016 2017
dbSNP: rs7937127
rs7937127
1 11 43493381 intron variant G/A snv 0.15 0.700 1.000 1 2017 2017