LMO7, LIM domain 7, 4008

N. diseases: 25; N. variants: 14
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: rs111870938
rs111870938
13 75680572 intron variant T/-;TT;TTT delins
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 1 2018 2018
dbSNP: rs7338461
rs7338461
13 75671406 intron variant G/A snv 0.41
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 1 2018 2018
dbSNP: rs9544020
rs9544020
13 75679111 intron variant A/G;T snv
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 1 2018 2018
dbSNP: rs9544022
rs9544022
13 75683130 intron variant G/A;C snv
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 1 2018 2018