Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs7609062

LRRFIP1

rs7609062 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRRFIP1. Location: chromosome 2, position 238,671,889. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

LRRFIP1Not classified
Variant type
synonymous_variant
Chromosome / position
2:238671889
HGVS
NM_001137552.2,c.1533G>A,p.Glu511Glu
Allele change
Silent

Public references

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