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: rs4554699
rs4554699
2 0.925 0.040 1 161638578 intergenic variant A/G snv 0.700 1.000 1 2018 2018
dbSNP: rs13239597
rs13239597
3 0.882 0.080 7 129055929 non coding transcript exon variant C/A snv 9.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs77583790
rs77583790
3 0.882 0.080 3 159976265 intron variant G/A;C snv 0.700 1.000 1 2014 2014
dbSNP: rs9373839
rs9373839
3 0.882 0.080 6 106207742 intron variant T/C snv 0.15 0.700 1.000 1 2014 2014
dbSNP: rs11642873
rs11642873
4 0.851 0.280 16 85958099 intergenic variant A/C snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs4543123
rs4543123
4 0.882 0.080 4 38790903 non coding transcript exon variant A/G snv 0.32 0.700 1.000 1 2018 2018
dbSNP: rs11893432
rs11893432
5 0.827 0.120 2 191057148 intron variant C/G snv 0.21 0.700 1.000 1 2018 2018
dbSNP: rs35677470
rs35677470
6 0.807 0.160 3 58197909 missense variant G/A;C snv 4.8E-02; 4.0E-06 0.700 1.000 1 2014 2014
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: rs10174238
rs10174238
14 0.724 0.200 2 191108308 intron variant G/A snv 0.70 0.700 1.000 1 2018 2018