Variant (rsID / SNP)

rs62270683

rs62270683 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR5H8, LOC105373999. Location: chromosome 3, position 98,030,869. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

OR5H8Not classified

Variant type: intragenic_variant
Chromosome / position: 3:98030869
HGVS: OR5H8,n.98030869C>T

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.