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: rs11656775
rs11656775
1 1.000 0.080 17 17751005 intron variant A/G snv 0.61 0.700 1.000 1 2017 2017
dbSNP: rs12945601
rs12945601
1 1.000 0.080 17 17750097 intron variant T/A;C snv 0.700 1.000 1 2018 2018