Variant (rsID / SNP)

rs3829765

rs3829765 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARMH4. Location: chromosome 14, position 58,605,790. The table records no clinical significance for this variant.

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Reference-table entries

ARMH4Not classified

Variant type: missense_variant
Chromosome / position: 14:58605790
HGVS: NM_001001872.4,c.287C>T,p.Thr96Ile
Allele change: Missense_T96I

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.