Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs805267

LY6G5B

rs805267 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LY6G5B. Location: chromosome 6, position 31,639,757. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

LY6G5BNot classified
Variant type
missense_variant
Chromosome / position
6:31639757
HGVS
NM_021221.3,c.304G>A,p.Asp102Asn
Allele change
Missense_D102N

Public references

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