ClinVar Miner

Variants from Human Evolutionary Genetics, Institut Pasteur

Location: France — Primary collection method: not provided
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 not provided total
0 0 0 0 0 539 539

Gene and significance breakdown #

Total genes and gene combinations: 30
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Gene or gene combination not provided total
NLRC5 68 68
NLRC3 37 37
NLRP5 32 32
NLRP6 32 32
NLRX1 29 29
NOD1 28 28
CIITA 27 27
NLRP2 24 24
IFNGR2 22 22
NLRP1 21 21
NOD2 21 21
NLRC4 20 20
IFNGR1 19 19
NLRP13 17 17
NLRP4 16 16
NLRP11 15 15
NLRP14 14 14
NLRP8 14 14
NLRP3 13 13
NLRP7 13 13
IFNGR2, TMEM50B 9 9
NLRP9 9 9
IFNG 8 8
NLRP10 8 8
NLRP12 6 6
TLR1 6 6
TLR6 6 6
NLRP11, NLRP4 2 2
TLR2 2 2
NCR1, NLRP7 1 1

Condition and significance breakdown #

Total conditions: 1
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Condition not provided total
not provided 539 539

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