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: rs758222990
rs758222990
1 1.000 0.080 17 39725363 missense variant C/G;T snv 1.2E-05 0.700 1.000 2 2006 2013