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Variant (rsID / SNP)

rs35972078

ARMT1

rs35972078 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARMT1. Location: chromosome 6, position 151,789,868. The table records no clinical significance for this variant.

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Reference-table entries

ARMT1Not classified
Variant type
missense_variant
Chromosome / position
6:151789868
HGVS
NM_024573.3,c.949G>A,p.Ala317Thr
Allele change
Missense_A198T

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.