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: rs2710383
rs2710383
1 1.000 0.040 22 32554983 intron variant G/C snv 0.11 0.700 1.000 1 2019 2019