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Variant (rsID / SNP)

rs201258323

NRXN2

rs201258323 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NRXN2. Location: chromosome 11, position 64,434,956. Clinical significance in the table: Uncertain significance.

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Reference-table entries

NRXN2Uncertain significance
Clinical significance (as recorded)
Uncertain significance
Variant type
single nucleotide variant
Chromosome / position
11:64434956
Cytoband
11q13.1
HGVS
NM_015080.4(NRXN2):c.1564C>T (p.Arg522Cys)
Allele change
Missense_R522C

Public references

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