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: rs10760442
rs10760442
1.000 0.040 9 126621621 intron variant G/A;T snv
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 1 2018 2018
dbSNP: rs3829849
rs3829849
9 126628521 intron variant C/T snv 0.28
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 1 2018 2018
dbSNP: rs6478750
rs6478750
9 126646919 intron variant T/C;G snv
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 1 2018 2018