ClinVar Miner

Variants from Epithelial Biology; Institute of Medical Biology, Singapore

Location: Singapore — 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 1094 1094

Gene and significance breakdown #

Total genes and gene combinations: 38
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Gene or gene combination not provided total
LMNA 289 289
KRT5 121 121
GFAP 103 103
KRT14 99 99
KRT1 60 60
DES 54 54
NEFL 43 43
KRT6A 37 37
KRT10, TMEM99 30 30
KRT9 27 27
LOC101927267, PRPH 24 24
KRT17 22 22
KRT8 22 22
KRT12 21 21
NEFH 21 21
KRT16 19 19
KRT2 14 14
NEFM 14 14
KRT18, LOC106096416 12 12
KRT86 10 10
KRT19 7 7
KRT13 6 6
KRT18, KRT8, LOC106096416 4 4
LMNB1 4 4
LMNB2 4 4
KRT10 3 3
KRT3 3 3
KRT6B 3 3
KRT74 3 3
KRT81, KRT86 3 3
BFSP2 2 2
KRT4 2 2
KRT6C 2 2
KRT83 2 2
CCDC103, GFAP 1 1
KRT75 1 1
KRT85 1 1
VIM 1 1

Condition and significance breakdown #

Total conditions: 1
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Condition not provided total
not provided 1094 1094

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