Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs11871553

MYO15B

rs11871553 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO15B. Location: chromosome 17, position 73,597,544. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

MYO15BNot classified
Variant type
missense_variant
Chromosome / position
17:73597544
HGVS
NM_001395058.1,c.3551A>G,p.Lys1184Arg
Allele change
Missense_K1146R

Public references

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