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: rs10194776
rs10194776
1 2 231115305 intron variant C/T snv 0.54 0.010 1.000 1 2014 2014
dbSNP: rs16827801
rs16827801
1 2 231116063 intron variant A/C;G snv 0.40 0.010 1.000 1 2014 2014