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: rs10152591
rs10152591
2 15 69755818 intron variant A/C snv 9.8E-02 0.700 1.000 1 2010 2010
dbSNP: rs16953685
rs16953685
1 15 69741749 intron variant A/C snv 0.10 0.700 1.000 1 2019 2019
dbSNP: rs34214868
rs34214868
1 15 69732152 intron variant -/C;CAAAAAC ins 0.700 1.000 1 2017 2017