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: rs111825958
rs111825958
2 19 40825304 intron variant C/A snv 3.5E-02 0.700 1.000 1 2018 2018
dbSNP: rs7507400
rs7507400
2 19 40824274 intron variant G/T snv 0.30 0.700 1.000 1 2016 2016