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: rs11840168
rs11840168
1 13 21544163 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs718426
rs718426
1 13 21511520 intron variant A/C;G snv 0.700 1.000 1 2018 2018