Variant (rsID / SNP)

rs17822931

rs17822931 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCC11. Location: chromosome 16, position 48,258,198. Clinical significance in the table: Benign.

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Reference-table entries

ABCC11Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 16:48258198
Cytoband: 16q12.1
HGVS: NM_001370497.1(ABCC11):c.538G>A (p.Gly180Arg)
Allele change: Missense_G180R

Associated conditions / phenotypes

Apocrine gland secretion, variation in|Axillary odor|Colostrum secretion

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.