Variant (rsID / SNP)

rs2641256

rs2641256 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCIMP. Location: chromosome 17, position 5,126,674. Clinical significance in the table: Uncertain_significance.

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Reference-table entries

SCIMPUncertain significance

Clinical significance (as recorded): Uncertain_significance
Variant type: synonymous_variant
Chromosome / position: 17:5126674
HGVS: NM_207103.3,c.99T>C,p.Gly33Gly
Allele change: Silent

Associated conditions / phenotypes

Squamous Cell Carcinoma, Head and Neck

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.