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: rs10734649
rs10734649
1 1.000 0.040 11 9759344 intron variant C/A;G;T snv 0.700 1.000 1 2018 2018