Variant (rsID / SNP)

rs17276250

rs17276250 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BDP1. Location: chromosome 5, position 70,858,268. Clinical significance in the table: Benign.

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Reference-table entries

BDP1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:70858268
Cytoband: 5q13.2
HGVS: NM_018429.3(BDP1):c.7664A>G (p.Asn2555Ser)
Allele change: Missense_N2555S

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.