Variant (rsID / SNP)

rs2071629

rs2071629 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYL2. Location: chromosome 12, position 111,351,186. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MYL2Not classified

Variant type: single nucleotide variant
Chromosome / position: 12:111351186
Cytoband: 12q24.11
HGVS: NM_000432.4(MYL2):c.275-58G>A
Allele change: Silent

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.