ClinVar Miner

Variants studied for X-linked osteoporosis with fractures

Included ClinVar conditions (1):
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 association total
3 0 0 0 1 3 7

Gene and significance breakdown #

Total genes and gene combinations: 3
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Gene or gene combination pathogenic benign association total
PLS3 1 0 3 4
HTR2C, IL13RA2, LRCH2, LUZP4, MIR448, PLS3, RBMXL3 2 0 0 2
G6PD 0 1 0 1

Submitter and significance breakdown #

Total submitters: 4
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Submitter pathogenic benign association total
OMIM 0 0 3 3
Baylor Miraca Genetics Laboratories, 2 0 0 2
Institute of Human Genetics,Cologne University 1 0 0 1
Department of Genetics,Sultan Qaboos University Hospital, Oman 0 1 0 1

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