Variant (rsID / SNP)

rs73714238

rs73714238 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC3A. Location: chromosome 7, position 100,551,626. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MUC3ANot classified

Variant type: missense_variant
Chromosome / position: 7:100551626
HGVS: NM_005960.2,c.2198T>C,p.Ile733Thr
Allele change: Missense_I736T

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.