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: rs62187537
rs62187537
1 20 1352416 intron variant C/T snv 6.7E-02 0.700 1.000 2 2019 2019
dbSNP: rs62187541
rs62187541
1 20 1359600 intron variant A/G snv 6.8E-02 0.700 1.000 1 2019 2019