LDB3, LIM domain binding 3, 11155

N. diseases: 69; N. variants: 15
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: rs121908333
rs121908333
1.000 10 86687163 missense variant G/A snv
CUI: C4721886
Disease: MYOPATHY, MYOFIBRILLAR, 4
MYOPATHY, MYOFIBRILLAR, 4
0.700 0
dbSNP: rs121908334
rs121908334
0.925 0.080 10 86687218 missense variant C/T snv 4.0E-06
CUI: C4721886
Disease: MYOPATHY, MYOFIBRILLAR, 4
MYOPATHY, MYOFIBRILLAR, 4
0.700 0