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: rs12670798
rs12670798
5 1.000 0.040 7 21567734 intron variant T/C snv 0.26 0.800 1.000 5 2009 2019
dbSNP: rs66476925
rs66476925
3 7 21571781 intron variant G/A;C;T snv 4.4E-06; 0.17; 4.4E-06 0.700 1.000 2 2019 2019
dbSNP: rs56130071
rs56130071
2 7 21559135 intron variant G/C snv 0.18 0.700 1.000 1 2015 2015
dbSNP: rs73066485
rs73066485
1 7 21572352 intron variant T/A;G snv 0.700 1.000 1 2018 2018