Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs4665830

GAREM2

rs4665830 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GAREM2. Location: chromosome 2, position 26,399,214. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

GAREM2Not classified
Variant type
splice_region_variant&synonymous_variant
Chromosome / position
2:26399214
HGVS
NM_001168241.2,c.114G>A,p.Gly38Gly
Allele change
Synonymous_G38G

Public references

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