Variant (rsID / SNP)

rs77326997

rs77326997 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL18A1, SLC19A1. Location: chromosome 21, position 46,930,155. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

COL18A1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 21:46930155
Cytoband: 21q22.3
HGVS: NM_001379500.1(COL18A1):c.3673G>A (p.Val1225Met)
Allele change: Missense_V1222M

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.