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: rs104893611
rs104893611
1 1.000 2 130597896 missense variant G/A snv 0.800 1.000 2 2000 2002
dbSNP: rs746231039
rs746231039
1 1.000 2 130593027 frameshift variant G/- del 8.1E-04 0.700 0
dbSNP: rs863223280
rs863223280
1 1.000 2 130597849 coding sequence variant -/ACCCCTGTGCCCACCTGCGC delins 0.700 0