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: rs10488631
rs10488631
13 0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs10516487
rs10516487
11 0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs11640251
rs11640251
1 1.000 0.040 16 70708633 intron variant G/A snv 0.49 0.700 1.000 1 2018 2018
dbSNP: rs17340351
rs17340351
2 0.925 0.040 7 129068743 upstream gene variant T/A snv 9.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs3733197
rs3733197
13 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 0.010 1.000 1 2009 2009