Variant (rsID / SNP)

rs6312

rs6312 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HTR2A. Location: chromosome 13, position 47,470,824. The table records no clinical significance for this variant.

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Reference-table entries

HTR2ANot classified

Variant type: 5_prime_UTR_variant
Chromosome / position: 13:47470824
HGVS: NM_000621.5,c.-344G>A
Allele change: Missense_D49N

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.