Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs6736609

MYO3B

rs6736609 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO3B. Location: chromosome 2, position 171,260,787. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

MYO3BNot classified
Variant type
missense_variant
Chromosome / position
2:171260787
HGVS
NM_138995.5,c.2308G>A,p.Val770Ile
Allele change
Missense_V770I

Public references

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