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Variant (rsID / SNP)

rs12443685

ABCC11

rs12443685 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCC11. Location: chromosome 16, position 48,226,479. The table records no clinical significance for this variant.

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Reference-table entries

ABCC11Not classified
Variant type
synonymous_variant
Chromosome / position
16:48226479
HGVS
NM_001370496.1,c.2664G>A,p.Lys888Lys
Allele change
Synonymous_K886K

Public references

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