ClinVar Miner

Variants from Department of Medical Genetics, Nizam's Institute of Medical Sciences

Location: India  Primary collection method: clinical testing
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign total
1 0 1 0 0 2

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic uncertain significance total
BMP4 0 1 1
TBX4 1 0 1

Condition and significance breakdown #

Total conditions: 2
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Condition pathogenic uncertain significance total
Aplasia/hypoplasia involving bones of the lower limbs; Absence of the sacrum 0 1 1
Hydronephrosis; Pulmonary hypoplasia; Hydroureter; Aplasia/hypoplasia involving bones of the lower limbs; Absence of the sacrum; Hypoplastic left heart syndrome 1 0 1

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