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: rs13191343
rs13191343
1 1.000 0.080 6 31273332 intron variant C/G;T snv 0.13 0.800 1.000 1 2010 2010