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: rs11121615
rs11121615
2 1.000 0.040 1 10765520 intron variant C/T snv 0.49 0.710 1.000 3 2018 2019