Variant (rsID / SNP)

rs3172008

rs3172008 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DRC1. Location: chromosome 2, position 26,678,040. The table records no clinical significance for this variant.

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Reference-table entries

DRC1Not classified

Variant type: missense_variant
Chromosome / position: 2:26678040
HGVS: NM_145038.5,c.2105G>T,p.Ser702Ile
Allele change: Missense_S702I

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.