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: rs6445541
rs6445541
1 1.000 0.040 3 52846112 intron variant G/T snv 0.37 0.700 1.000 1 2018 2018
dbSNP: rs9836178
rs9836178
1 1.000 0.040 3 52891387 intron variant T/A;C snv 0.700 1.000 1 2018 2018