Variant (rsID / SNP)

rs10985112

rs10985112 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C5. Location: chromosome 9, position 123,731,408. Clinical significance in the table: Benign.

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Reference-table entries

C5Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 9:123731408
Cytoband: 9q33.2
HGVS: NM_001735.3(C5):c.4163-12C>T
Allele change: Silent

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.