Variant (rsID / SNP)

rs41307798

rs41307798 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CTRC. Location: chromosome 1, position 15,768,997. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

CTRCBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:15768997
Cytoband: 1p36.21
HGVS: NM_007272.3(CTRC):c.285C>T (p.Asp95=)
Allele change: Synonymous_D95D

Associated conditions / phenotypes

Hereditary pancreatitis|Inborn genetic diseases

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.