Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7635832
rs7635832
3 172271486 intron variant T/G snv 0.22
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 3 2017 2018
dbSNP: rs12492846
rs12492846
3 172208901 intron variant C/T snv 0.73
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 2 2018 2018
dbSNP: rs6445055
rs6445055
0.925 0.040 3 172274597 intron variant G/A snv 0.24
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 2 2014 2017
dbSNP: rs16856911
rs16856911
3 172082708 intron variant G/C snv 5.8E-02
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 1 2018 2018
dbSNP: rs4380442
rs4380442
3 172212591 intron variant G/A snv 0.90
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 1 2018 2018
dbSNP: rs62283814
rs62283814
3 172103766 intron variant C/T snv 0.18
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 1 2018 2018