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: rs3757769
rs3757769
2 1.000 0.080 7 127901009 intron variant A/G snv 9.7E-02 0.010 1.000 1 2020 2020
dbSNP: rs7778413
rs7778413
2 1.000 0.080 7 127717662 intron variant T/C snv 0.23 0.010 1.000 1 2020 2020