ClinVar Miner

Variants from Department of Prosthodontics, Peking University School and Hospital of Stomatology

Location: China  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
23 5 5 0 0 33

Gene and significance breakdown #

Total genes and gene combinations: 12
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Gene or gene combination pathogenic likely pathogenic uncertain significance total
WNT10A 5 2 1 8
EDAR, RANBP2 7 0 0 7
PAX9 3 0 1 4
LRP6 3 0 0 3
BMP4 0 0 2 2
BMPR2 0 2 0 2
EDA 2 0 0 2
AXIN2 1 0 0 1
CDH1 0 1 0 1
DLX3 1 0 0 1
KDF1 0 0 1 1
MSX1 1 0 0 1

Condition and significance breakdown #

Total conditions: 12
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Condition pathogenic likely pathogenic uncertain significance total
Non-syndromic oligodontia 8 0 0 8
Odonto-onycho-dermal dysplasia 5 0 0 5
Tooth agenesis, selective, 3 3 0 1 4
Tooth agenesis, selective, 1 1 2 0 3
Tooth agenesis, selective, 4 0 2 1 3
Tooth agenesis, selective, 7 3 0 0 3
Hypohidrotic X-linked ectodermal dysplasia 2 0 0 2
Blepharocheilodontic syndrome 1 0 1 0 1
Partial congenital absence of teeth 0 0 1 1
Tooth agenesis 0 0 1 1
Tooth agenesis; Low bone mineral density 0 0 1 1
Tricho-dento-osseous syndrome 1 0 0 1

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