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: rs779989663
rs779989663
2 0.925 0.040 16 9841092 missense variant A/T snv 4.8E-05 7.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs796052549
rs796052549
2 0.925 0.040 16 9798442 missense variant C/G;T snv 0.010 1.000 1 2017 2017