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: rs17026156
rs17026156
1 2 40533825 intron variant T/C snv 6.8E-02 0.700 1.000 2 2014 2019
dbSNP: rs4952632
rs4952632
1 2 40520865 intron variant T/G snv 8.5E-02 0.700 1.000 2 2014 2019
dbSNP: rs17026148
rs17026148
1 2 40530430 intron variant G/A snv 9.1E-02 0.700 1.000 1 2018 2018