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Variant (rsID / SNP)

rs138213197

HOXB13

rs138213197 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HOXB13. Location: chromosome 17, position 46,805,705. Clinical significance in the table: Conflicting interpretations of pathogenicity; association.

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Reference-table entries

HOXB13Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity; association
Variant type
single nucleotide variant
Chromosome / position
17:46805705
Cytoband
17q21.32
HGVS
NM_006361.6(HOXB13):c.251G>A (p.Gly84Glu)
Allele change
Missense_G84E

Associated conditions / phenotypes

Prostate cancer susceptibility|Hereditary cancer-predisposing syndrome|Prostate cancer, hereditary, 9|Carcinoma of pancreas|Familial prostate carcinoma

Public references

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