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: rs794726864
rs794726864
1 1.000 0.120 12 20616294 missense variant C/A;G snv 0.800 0
dbSNP: rs794726865
rs794726865
1 1.000 0.120 12 20616293 missense variant A/G snv 0.800 0
dbSNP: rs794726866
rs794726866
1 1.000 0.120 12 20616299 missense variant G/A snv 0.800 0
dbSNP: rs794726867
rs794726867
1 1.000 0.120 12 20616300 missense variant C/T snv 0.800 0
dbSNP: rs794726868
rs794726868
1 1.000 0.120 12 20616306 missense variant G/T snv 0.800 0