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: rs35260355
rs35260355
2 1.000 0.080 1 33480230 intron variant C/G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs71647933
rs71647933
2 1.000 0.080 1 33480000 intron variant A/G;T snv 0.700 1.000 1 2015 2015