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Variant (rsID / SNP)

rs11568591

ABCC3

rs11568591 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCC3. Location: chromosome 17, position 48,761,053. The table records no clinical significance for this variant.

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Reference-table entries

ABCC3Not classified
Variant type
missense_variant
Chromosome / position
17:48761053
HGVS
NM_003786.4,c.3890G>A,p.Arg1297His
Allele change
Missense_R1297H

Public references

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