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: rs12330322
rs12330322
2 3 72406204 intron variant C/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs6549455
rs6549455
1 3 72408070 intron variant A/G snv 0.59 0.700 1.000 1 2017 2017
dbSNP: rs7628338
rs7628338
1 3 72383737 intron variant G/A snv 0.58 0.700 1.000 1 2017 2017