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: rs10516487
rs10516487
11 0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 0.880 1.000 9 2008 2019
dbSNP: rs17266594
rs17266594
7 0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 0.850 1.000 7 2008 2017
dbSNP: rs10028805
rs10028805
3 0.882 0.160 4 101816093 intron variant G/A snv 0.45 0.700 1.000 1 2015 2015
dbSNP: rs4426778
rs4426778
1 1.000 0.080 4 101859567 intron variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs4637409
rs4637409
1 1.000 0.080 4 101832251 intron variant A/G snv 0.27 0.700 1.000 1 2017 2017
dbSNP: rs3733197
rs3733197
13 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 0.040 1.000 4 2009 2019
dbSNP: rs4522865
rs4522865
4 0.882 0.240 4 101794731 intron variant G/A;T snv 0.010 1.000 1 2009 2009