Variant (rsID / SNP)

rs140556296

rs140556296 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CHRNB1. Location: chromosome 17, position 7,349,418. Clinical significance in the table: Uncertain significance.

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Reference-table entries

CHRNB1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 17:7349418
Cytoband: 17p13.1
HGVS: NM_000747.3(CHRNB1):c.229G>T (p.Val77Leu)
Allele change: Missense_V77M

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.