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: rs2929282
rs2929282
2 15 43953733 intron variant A/T snv 0.13 0.800 1.000 5 2010 2019
dbSNP: rs138570705
rs138570705
2 15 43974532 intron variant G/A snv 2.0E-02 0.700 1.000 3 2015 2019
dbSNP: rs481837
rs481837
2 15 43925938 intron variant C/T snv 9.5E-02 0.700 1.000 1 2018 2018
dbSNP: rs492571
rs492571
2 15 43919075 5 prime UTR variant T/C snv 8.2E-02 0.700 1.000 1 2019 2019