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: rs224330
rs224330
2 20 35434398 synonymous variant T/C snv 0.90 0.700 1.000 1 2010 2010
dbSNP: rs224332
rs224332
2 20 35434874 missense variant A/C;G snv 0.700 1.000 1 2010 2010
dbSNP: rs224334
rs224334
2 20 35436939 intron variant A/G snv 0.92 0.700 1.000 1 2010 2010
dbSNP: rs739329
rs739329
2 20 35439830 intron variant G/A snv 3.0E-02 0.700 1.000 1 2010 2010