Variant (rsID / SNP)

rs2074877

rs2074877 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH13. Location: chromosome 17, position 10,223,714. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MYH13Not classified

Variant type: missense_variant
Chromosome / position: 17:10223714
HGVS: NM_003802.3,c.3211A>G,p.Met1071Val
Allele change: Missense_M1071V

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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