Variant (rsID / SNP)
rs1799929
rs1799929 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NAT2. Location: chromosome 8, position 18,257,994. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- synonymous_variant
- Chromosome / position
- 8:18257994
- HGVS
- NM_000015.3,c.481C>T,p.Leu161Leu
- Allele change
- Synonymous_L161L
Associated conditions / phenotypes
Mycobacterium Tuberculosis 1|Male Infertility|Infertility|Psoriasis 1|Leukemia|Skin Disease|Pustulosis of Palm and Sole|Psoriasis|Cleft Palate, Isolated|Childhood Acute Lymphocytic Leukemia|Leukemia, Acute Lymphoblastic|Acetylation, Slow|Cleft Lip|Oral Cancer|Endometriosis|Childhood Leukemia|Cleft Lip with or Without Cleft Palate|Acute Leukemia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.