Variant (rsID / SNP)

rs11150624

rs11150624 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARMC5. Location: chromosome 16, position 31,476,458. The table records no clinical significance for this variant.

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Reference-table entries

ARMC5Not classified

Variant type: missense_variant
Chromosome / position: 16:31476458
HGVS: NM_024742.2,c.2114C>T,p.Ala705Val
Allele change: Silent

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.