Variant (rsID / SNP)

rs41271969

rs41271969 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NOS1AP. Location: chromosome 1, position 162,302,846. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

NOS1APBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:162302846
Cytoband: 1q23.3
HGVS: NM_014697.3(NOS1AP):c.384C>T (p.Ile128=)
Allele change: Synonymous_I123I

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.