Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs7761137

CAPN11

rs7761137 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CAPN11. Location: chromosome 6, position 44,151,490. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

CAPN11Not classified
Variant type
missense_variant
Chromosome / position
6:44151490
HGVS
NM_007058.4,c.2183G>A,p.Ser728Asn
Allele change
Missense_S728N

Public references

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