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: rs10817758
rs10817758
1 1.000 0.040 9 115381654 intron variant C/T snv 0.13 0.700 1.000 1 2015 2015