Variant (rsID / SNP)

rs6416668

rs6416668 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCC6. Location: chromosome 16, position 16,271,357. The table records no clinical significance for this variant.

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Reference-table entries

ABCC6Not classified

Variant type: missense_variant
Chromosome / position: 16:16271357
HGVS: NM_001171.6,c.2542A>G,p.Met848Val
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.