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: rs11127126
rs11127126
1 2 27800417 intron variant C/T snv 0.36 0.700 1.000 1 2019 2019
dbSNP: rs4630723
rs4630723
1 2 27801464 intron variant T/C snv 0.21 0.700 1.000 1 2018 2018