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: rs10195136
rs10195136
2 0.925 0.040 2 115797465 intron variant T/C snv 6.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs12711836
rs12711836
2 0.925 0.040 2 115824811 intron variant G/A snv 0.97 0.700 1.000 1 2018 2018