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: rs11253511
rs11253511
1 10 918892 intron variant C/T snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs12264390
rs12264390
2 10 913171 intron variant T/C snv 0.20 0.700 1.000 1 2016 2016