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Variant (rsID / SNP)

rs9223

NPAS2

rs9223 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NPAS2. Location: chromosome 2, position 101,609,827. The table records no clinical significance for this variant.

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Reference-table entries

NPAS2Not classified
Variant type
synonymous_variant
Chromosome / position
2:101609827
HGVS
NM_002518.4,c.2130C>T,p.Thr710Thr
Allele change
Synonymous_T710T

Public references

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