Disease: Tonometry ×
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: rs11217878
rs11217878 		1.000 0.040 11 120469674 intron variant G/A snv 0.20
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 3 2015 2018
dbSNP: rs11217863
rs11217863 		11 120422429 intron variant G/A snv 8.6E-02
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 2 2015 2018
dbSNP: rs12794618
rs12794618 		11 120418990 intron variant T/C snv 0.21
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 2 2015 2017
dbSNP: rs10502235
rs10502235 		11 120341714 intron variant A/G snv 0.19
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2015 2015
dbSNP: rs10790381
rs10790381 		11 120386786 intron variant A/G snv 0.20
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2015 2015
dbSNP: rs10892565
rs10892565 		11 120364851 intron variant T/C snv 0.21
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2015 2015
dbSNP: rs10892569
rs10892569 		11 120399540 intron variant A/G snv 0.19
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2015 2015
dbSNP: rs10892575
rs10892575 		11 120420428 intron variant C/G snv 0.20
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2015 2015
dbSNP: rs11217843
rs11217843 		11 120369228 intron variant A/G snv 0.20
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2015 2015
dbSNP: rs11217857
rs11217857 		11 120399461 intron variant A/G snv 0.21
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2015 2015
dbSNP: rs11217866
rs11217866 		11 120430095 intron variant T/A snv 0.20
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2015 2015
dbSNP: rs11217874
rs11217874 		11 120454839 intron variant G/A;T snv
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2015 2015
dbSNP: rs11217875
rs11217875 		11 120454850 intron variant C/A;T snv
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2015 2015
dbSNP: rs11823264
rs11823264 		11 120423295 intron variant G/A snv 0.20
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2015 2015
dbSNP: rs11824032
rs11824032 		11 120354080 intron variant G/A;T snv
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2015 2015
dbSNP: rs12270397
rs12270397 		11 120377633 intron variant C/T snv 0.21
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2015 2015
dbSNP: rs12785387
rs12785387 		11 120351278 intron variant C/G;T snv
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2015 2015
dbSNP: rs12807097
rs12807097 		11 120371639 intron variant G/A snv 0.19
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2015 2015
dbSNP: rs17123861
rs17123861 		11 120385628 intron variant T/C snv 0.21
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2015 2015
dbSNP: rs1812974
rs1812974 		11 120350359 intron variant C/T snv 0.21
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2015 2015
dbSNP: rs199800298
rs199800298 		11 120477875 intron variant G/- del 2.3E-03
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2017 2017
dbSNP: rs2276035
rs2276035 		11 120475651 intron variant G/A snv 0.20
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2015 2015
dbSNP: rs2305013
rs2305013 		11 120469351 missense variant A/G;T snv 6.2E-02 4.2E-02
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs4936518
rs4936518 		11 120440489 intron variant A/T snv 0.21
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2015 2015
dbSNP: rs4938802
rs4938802 		11 120358280 intron variant A/G snv 0.19
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2015 2015