CDH11, cadherin 11, 1009

N. diseases: 203; N. variants: 9
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: rs1874458
rs1874458
16 65046836 intron variant G/A snv 0.26
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 2 2018 2018
dbSNP: rs35195
rs35195
16 64991815 missense variant G/A snv 0.27 0.25
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 1 2018 2018
dbSNP: rs564626594
rs564626594
16 65021636 intron variant -/G ins
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 1 2018 2018