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: rs7134594
rs7134594
2 1.000 0.200 12 109562388 intron variant C/G;T snv 0.800 1.000 2 2010 2019