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Variant (rsID / SNP)

rs11866251

ABCC11

rs11866251 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCC11. Location: chromosome 16, position 48,227,862. The table records no clinical significance for this variant.

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Reference-table entries

ABCC11Not classified
Variant type
synonymous_variant
Chromosome / position
16:48227862
HGVS
NM_001370496.1,c.2442C>T,p.Phe814Phe
Allele change
Synonymous_F812F

Public references

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