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Variant (rsID / SNP)

rs2305160

NPAS2

rs2305160 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NPAS2. Location: chromosome 2, position 101,591,304. The table records no clinical significance for this variant.

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Reference-table entries

NPAS2Not classified
Variant type
missense_variant
Chromosome / position
2:101591304
HGVS
NM_002518.4,c.1180A>G,p.Thr394Ala
Allele change
Missense_T394A

Associated conditions / phenotypes

Leukemia, Chronic Lymphocytic|Major Depressive Disorder|Restless Legs Syndrome|Schizophrenia|Insulin-Like Growth Factor I|B-Cell Lymphoma|Mood Disorder

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.