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: rs323167
rs323167
1 1.000 0.040 7 78707361 intron variant C/T snv 0.68 0.700 1.000 1 2017 2017
dbSNP: rs4727751
rs4727751
1 1.000 0.040 7 78707618 intron variant T/G snv 0.41 0.700 1.000 1 2015 2015