Variant (rsID / SNP)

rs2259292

rs2259292 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC4. Location: chromosome 3, position 195,501,149. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MUC4Not classified

Variant type: missense_variant
Chromosome / position: 3:195501149
HGVS: NM_018406.7,c.12971G>A,p.Gly4324Asp
Allele change: Missense_A3586T

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.