Variant (rsID / SNP)

rs138338446

rs138338446 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CFTR. Location: chromosome 7, position 117,175,323. Clinical significance in the table: Uncertain significance.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

CFTRUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 7:117175323
Cytoband: 7q31.2
HGVS: NM_000492.4(CFTR):c.601G>A (p.Val201Met)
Allele change: Missense_V201M

Associated conditions / phenotypes

Cystic fibrosis|Inborn genetic diseases|CFTR-related disorders|Hereditary pancreatitis

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.