Variant (rsID / SNP)

rs3747350

rs3747350 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NDP. Clinical significance in the table: Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

NDPLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Cytoband: Xp11.3
HGVS: NM_000266.4(NDP):c.*715T>C
Allele change: Silent

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.