Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs3760423

MYH13

rs3760423 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH13. Location: chromosome 17, position 10,243,717. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

MYH13Not classified
Variant type
splice_region_variant&synonymous_variant
Chromosome / position
17:10243717
HGVS
NM_003802.3,c.1896C>T,p.Gly632Gly
Allele change
Synonymous_G632G

Public references

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