Variant (rsID / SNP)

rs121908982

rs121908982 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAD1L1. Location: chromosome 7, position 2,265,161. Clinical significance in the table: Pathogenic.

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Reference-table entries

MAD1L1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 7:2265161
Cytoband: 7p22.3
HGVS: NM_001013836.2(MAD1L1):c.175C>T (p.Arg59Cys)
Allele change: Missense_R59C

Associated conditions / phenotypes

Prostate cancer, somatic

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.