Variant (rsID / SNP)

rs10993994

rs10993994 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MSMB. Location: chromosome 10, position 51,549,496. Clinical significance in the table: risk factor.

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Reference-table entries

MSMBRisk factor

Clinical significance (as recorded): risk factor
Variant type: single nucleotide variant
Chromosome / position: 10:51549496
Cytoband: 10q11.22
HGVS: NM_002443.3(MSMB):c.-89T=
Allele change: Silent

Associated conditions / phenotypes

Prostate cancer, hereditary, 13

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.