Variant (rsID / SNP)

rs35394227

rs35394227 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NLGN4Y. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

NLGN4YBenign

Clinical significance (as recorded): Benign
Variant type: synonymous_variant
HGVS: NM_001365584.1,c.699C>T,p.Thr233Thr
Allele change: Synonymous_T45T

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.