Variant (rsID / SNP)

rs61742367

rs61742367 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CIDEC. Location: chromosome 3, position 9,918,811. Clinical significance in the table: Benign.

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Reference-table entries

CIDECBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:9918811
Cytoband: 3p25.3
HGVS: NM_001321142.2(CIDEC):c.146C>T (p.Thr49Met)
Allele change: Missense_T62M

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.