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Variant (rsID / SNP)

rs61739606

ABCC11

rs61739606 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCC11. Location: chromosome 16, position 48,204,078. The table records no clinical significance for this variant.

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Reference-table entries

ABCC11Not classified
Variant type
missense_variant
Chromosome / position
16:48204078
HGVS
NM_001370496.1,c.3835A>T,p.Asn1279Tyr
Allele change
Missense_N1277Y

Public references

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