Variant (rsID / SNP)

rs3752087

rs3752087 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAPK4. Location: chromosome 18, position 48,190,440. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MAPK4Not classified

Variant type: missense_variant
Chromosome / position: 18:48190440
HGVS: NM_002747.4,c.112G>A,p.Val38Met
Allele change: Missense_V38M

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.