Variant (rsID / SNP)

rs41321249

rs41321249 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ITGAM. Location: chromosome 16, position 31,341,424. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ITGAMBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 16:31341424
Cytoband: 16p11.2
HGVS: NM_000632.4(ITGAM):c.2999C>A (p.Thr1000Asn)
Allele change: Missense_T1001N

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.