Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs16980994

OR10H4

rs16980994 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR10H4. Location: chromosome 19, position 16,060,117. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

OR10H4Not classified
Variant type
missense_variant
Chromosome / position
19:16060117
HGVS
NM_001004465.1,c.300C>A,p.Asn100Lys
Allele change
Missense_N100K

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.