Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs7646919

NLGN1

rs7646919 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NLGN1. Location: chromosome 3, position 173,997,153. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

NLGN1Not classified
Variant type
synonymous_variant
Chromosome / position
3:173997153
HGVS
NM_001365923.2,c.1422G>A,p.Lys474Lys
Allele change
Synonymous_K454K

Public references

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