Variant (rsID / SNP)

rs4729631

rs4729631 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC12. Location: chromosome 7, position 100,635,205. The table records no clinical significance for this variant.

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Reference-table entries

MUC12Not classified

Variant type: missense_variant
Chromosome / position: 7:100635205
HGVS: NM_001164462.2,c.1361C>T,p.Ala454Val
Allele change: Missense_A454V

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.