Variant (rsID / SNP)

rs6295

rs6295 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HTR1A. Location: chromosome 5, position 63,258,565. Clinical significance in the table: Benign.

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Reference-table entries

HTR1ABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:63258565
Cytoband: 5q12.3
HGVS: NM_000524.3(HTR1A):c.-1019G>G

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.