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: rs2282018
rs2282018
AVP
1 1.000 0.040 20 3084303 intron variant C/T snv 0.60 0.010 1.000 1 2016 2016
dbSNP: rs6084264
rs6084264
AVP
1 1.000 0.040 20 3089925 upstream gene variant T/C snv 0.58 0.010 1.000 1 2016 2016