NHLRC2 Chromosome 10
NHL repeat containing 2
Upload your DNA to see your personal genotypes for variants in NHLRC2.
What This Gene Does
Located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Associated Conditions (9)
Inborn genetic diseases
NHLRC2-related disorder
Fibrosis
neurodegeneration
and cerebral angiomatosis
Familial cancer of breast
Clear cell carcinoma of kidney
See cases
Melanoma
Key Variants
RS144606661
Conflicting classifications of pathogenicity
Inborn genetic diseases, NHLRC2-related disorder, Inborn genetic diseases
Health Risk
RS148376909
Conflicting classifications of pathogenicity
Inborn genetic diseases, Fibrosis, neurodegeneration
Health Risk
RS150975627
Conflicting classifications of pathogenicity
Inborn genetic diseases, NHLRC2-related disorder, Clear cell carcinoma of kidney
Health Risk
RS2134678958
Conflicting classifications of pathogenicity
Fibrosis, neurodegeneration, and cerebral angiomatosis
Health Risk
RS2494421263
Likely pathogenic
Fibrosis, neurodegeneration, and cerebral angiomatosis
Health Risk
RS747117082
Likely pathogenic
See cases, See cases
Health Risk
RS1425674152
Pathogenic
Fibrosis, neurodegeneration, and cerebral angiomatosis
Health Risk
RS1488953322
Pathogenic
Fibrosis, neurodegeneration, and cerebral angiomatosis
Health Risk
RS1846062683
Pathogenic
Fibrosis, neurodegeneration, and cerebral angiomatosis
Health Risk
RS201701259
Pathogenic
Fibrosis, neurodegeneration, and cerebral angiomatosis
Health Risk
RS2134706667
Pathogenic
Fibrosis, neurodegeneration, and cerebral angiomatosis
Health Risk
RS757267294
Pathogenic
Fibrosis, neurodegeneration, and cerebral angiomatosis
Health Risk
All Variants (12)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS144606661 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, NHLRC2-related disorder, Inborn genetic diseases |
| RS148376909 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Fibrosis, neurodegeneration |
| RS150975627 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, NHLRC2-related disorder, Clear cell carcinoma of kidney |
| RS2134678958 | Health Risk | Conflicting classifications of pathogenicity | Fibrosis, neurodegeneration, and cerebral angiomatosis |
| RS2494421263 | Health Risk | Likely pathogenic | Fibrosis, neurodegeneration, and cerebral angiomatosis |
| RS747117082 | Health Risk | Likely pathogenic | See cases, See cases |
| RS1425674152 | Health Risk | Pathogenic | Fibrosis, neurodegeneration, and cerebral angiomatosis |
| RS1488953322 | Health Risk | Pathogenic | Fibrosis, neurodegeneration, and cerebral angiomatosis |
| RS1846062683 | Health Risk | Pathogenic | Fibrosis, neurodegeneration, and cerebral angiomatosis |
| RS201701259 | Health Risk | Pathogenic | Fibrosis, neurodegeneration, and cerebral angiomatosis |
| RS2134706667 | Health Risk | Pathogenic | Fibrosis, neurodegeneration, and cerebral angiomatosis |
| RS757267294 | Health Risk | Pathogenic | Fibrosis, neurodegeneration, and cerebral angiomatosis |