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: rs13429458
rs13429458
1 0.827 0.200 2 43411699 intron variant A/C snv 0.14 0.890 0.800 2 2011 2019
dbSNP: rs12478601
rs12478601
1 0.851 0.200 2 43494369 intron variant C/T snv 0.61 0.820 0.750 1 2011 2019
dbSNP: rs7563201
rs7563201
1 1.000 0.120 2 43334641 intron variant G/A snv 0.45 0.700 1.000 2 2015 2018