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: rs11772848
rs11772848
7 101400749 intron variant G/A snv 0.22
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 1 2018 2018
dbSNP: rs62465642
rs62465642
7 101414212 intron variant A/C snv 0.17
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 1 2018 2018