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MSeqDR_General
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Clinician Mode
Genomic Search
Disease: OMIM
Disease: HPO
Examples Gene:
MT-ND1
,
POLG
, Region:
M:1-1000
Variant:
m.8993T>G
,
1:g.10042757T>C
rs3888511
MSCV_0000006
, ClinVar:
RCV000000015
, Disease:
Leigh syndrome
, Phenotype:
Retinopathy
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