Variant (rsID / SNP)

rs187397245

rs187397245 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NRXN2. Location: chromosome 11, position 64,415,726. 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: 11:64415726
Cytoband: 11q13.1
HGVS: NM_015080.4(NRXN2):c.3368C>T (p.Thr1123Ile)
Allele change: Missense_T1123I

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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