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: rs28931575
rs28931575
1 1.000 11 116836271 missense variant A/G snv 0.700 0
dbSNP: rs387906571
rs387906571
2 0.925 0.120 11 116836094 missense variant C/G snv 0.700 0