Variant (rsID / SNP)

rs1983546

rs1983546 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC19A2. Location: chromosome 1, position 169,446,183. Clinical significance in the table: Benign.

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Reference-table entries

SLC19A2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:169446183
Cytoband: 1q24.2
HGVS: NM_006996.3(SLC19A2):c.807+210T>C
Allele change: Silent

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.