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: rs867186
rs867186
15 0.752 0.120 20 35176751 missense variant A/G snv 0.10 9.7E-02 0.710 1.000 2 2010 2019
dbSNP: rs10747514
rs10747514
1 20 35187566 intron variant G/A snv 0.40 0.700 1.000 1 2019 2019
dbSNP: rs34234989
rs34234989
5 0.882 0.120 20 35186731 intron variant A/- delins 0.40 0.700 1.000 1 2016 2016
dbSNP: rs6060288
rs6060288
1 20 35184440 intron variant G/A snv 0.40 0.700 1.000 1 2019 2019
dbSNP: rs6087685
rs6087685
3 20 35189809 intron variant G/C snv 0.40 0.700 1.000 1 2015 2015