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: rs879255639
rs879255639
3 0.882 0.040 7 128848926 missense variant C/T snv 0.700 0
dbSNP: rs879255640
rs879255640
3 0.882 0.040 7 128853831 missense variant A/T snv 0.700 0